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Study | ONLINE FIRST

Calcinosis Cutis Occurring in Association With Autoimmune Connective Tissue Disease:  The Mayo Clinic Experience With 78 Patients, 1996-2009 FREE

Samuel J. Balin, PhD; David A. Wetter, MD; Louise K. Andersen, MD; Mark D. P. Davis, MD
[+] Author Affiliations

Author Affiliations: Department of Dermatology, Mayo Clinic, Rochester, Minnesota (Drs Wetter, Andersen, and Davis). Dr Balin was a medical student at Mayo Medical School, College of Medicine, Mayo Clinic. Dr Balin is now with the Department of Internal Medicine, Albert Einstein College of Medicine, Jacobi Medical Center, Bronx, New York.


Arch Dermatol. 2012;148(4):455-462. doi:10.1001/archdermatol.2011.2052.
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Objective To describe characteristics and treatment of patients with calcinosis cutis in the clinical setting of autoimmune connective tissue disease (ACTD).

Design Retrospective study.

Setting Tertiary referral center.

Patients Seventy-eight patients with calcinosis cutis and ACTD between 1996 and 2009.

Main Outcome Measures Clinical features, treatments, and outcomes of patients with calcinosis cutis in the clinical setting of ACTD.

Results Of 78 patients (mean age at onset of calcinosis cutis, 40.1 years), 64 (82%) were female. The following diseases were associated with calcinosis cutis: dermatomyositis (n = 30) with classic (n = 15), juvenile (n = 14), and amyopathic (n = 1) subtypes; systemic sclerosis with limited cutaneous scleroderma (n = 24); lupus panniculitis (n = 4); systemic lupus erythematosus (n = 2); mixed connective tissue disease (n = 4); overlap connective tissue disease (n = 6); undifferentiated connective tissue disease (n = 6); polymyositis (n = 1); and rheumatoid arthritis (n = 1). Therapy for calcinosis cutis consisted of medical treatment alone (n = 19), surgical therapy alone (n = 11), combined medical and surgical treatment (n = 17), no treatment (n = 30), and unknown (n = 1). Diltiazem hydrochloride was the most commonly used medical therapy, with 9 of 17 patients having a partial response. Twenty-eight patients had surgical excision of 1 or more lesions of calcinosis cutis: 22 had a complete response, 5 had a partial response, and 1 had no response.

Conclusions Dermatomyositis and systemic sclerosis were the most common ACTDs associated with calcinosis cutis. Although no treatment was uniformly effective, surgical excision of symptomatic lesions and medical treatment with diltiazem provided benefit for some patients.

Figures in this Article

Four subtypes of calcinosis cutis exist: dystrophic, metastatic, iatrogenic, and idiopathic.1,2 Of these subtypes, dystrophic calcinosis cutis is the most common, and it is most frequently seen in association with underlying autoimmune connective tissue disease (ACTD).1 The condition causes substantial morbidity and is associated with pain when the process involves areas close to joints or when ulceration occurs. Because of this substantial morbidity, treatment is often sought; however, the condition is exceedingly hard to treat.3,4 Descriptions of patients with calcinosis cutis in the clinical setting of underlying ACTD and their treatments have thus far been limited to small case series and case reports.

The objectives of this study were to elucidate the ACTDs associated with calcinosis cutis in a series of 78 patients seen at Mayo Clinic, Rochester, Minnesota, and to describe the clinical features, treatments, and outcomes of these patients.

DATA COLLECTION

We used the institutional medical index and text retrieval system to identify patients who received a diagnosis of (1) calcinosis cutis, cutaneous calcification, or calcinosis and (2) connective tissue disease, dermatomyositis, lupus, scleroderma, or systemic sclerosis at Mayo Clinic between January 1, 1996, and December 31, 2009. Patients who denied research authorization were excluded from the study. This study was approved by the Mayo Clinic Institutional Review Board.

The initial search identified 923 patients, and we examined the medical records of these patients to identify 78 who met the study inclusion criteria of calcinosis cutis occurring in association with ACTD. Patients who did not meet the criteria for ACTD were excluded. Patients with incidentally identified forms of calcinosis that were unrelated to ACTD (eg, cutaneous neoplasms with foci of calcification present on histopathologic examination and benign breast calcification identified on mammography) also were excluded. For this study, overlap connective tissue disease (CTD) was defined as 2 or more separate ACTDs where each disease complied with the classification criteria for that disorder.5 Similarly, we defined undifferentiated CTD as ACTD that had clinical or serologic features, or both, of CTD but had not yet developed into defined disease and did not meet the classification criteria for a particular disorder.5

We abstracted the following information from the medical records of the 78 patients: patient characteristics (eg, sex and age), disease duration, clinical characteristics of calcinosis cutis (eg, pain, ulceration, and extent and location of the calcinosis), underlying ACTD, duration of ACTD until the onset of calcinosis cutis, histopathologic and imaging findings of calcinosis cutis, treatments used for the associated ACTD, treatments used for calcinosis cutis, response to treatments, and follow-up data since diagnosis.

RESPONSE TO THERAPY

Patient response to therapy was graded according to the response levels of complete, partial, none, or unknown. Total resolution of an individual lesion and lack of recurrence in that area indicated complete response. Regression or recurrence of a lesion that had previously regressed or completely healed indicated partial response. The persistence of old lesions with or without the occurrence of new lesions indicated no response.

STATISTICAL ANALYSIS

Overall survival rates were estimated using the Kaplan-Meier method and were compared with the expected survival of age- and sex-matched Minnesota residents through a log-rank test. Comparisons among the number of calcinosis locations, of therapies for calcinosis, and of therapies for CTD were evaluated using the Kruskal-Wallis test and Spearman rank correlation coefficients. All tests were 2 sided, and P < .05 was considered statistically significant.

PATIENT DEMOGRAPHIC CHARACTERISTICS AND UNDERLYING ACTD

Table 1 summarizes the age at onset and the sex of the 78 study patients by underlying ACTD. The mean patient age at the onset of calcinosis cutis was 40.1 years (range, 4-75 years). Sixty-four patients (82%) were female and 14 (18%) were male. Table 1 also provides the mean time to development of calcinosis cutis by underlying ACTD. The duration of ACTD until the onset of calcinosis cutis varied among the underlying diseases.

Table Graphic Jump LocationTable 1. Characteristics and Prevalence of ACTD Associated With Calcinosis Cutis
CALCINOSIS CUTIS LOCATIONS

Locations of calcinosis cutis were classified as the head, extremity (including the buttocks but excluding the hands and feet), trunk, and hands or feet (Figure 1). The location of calcinosis cutis differed on the basis of the underlying ACTD in which the calcinosis occurred (Table 2). Forty-three patients (55%) had ulcer formation in the context of calcinosis cutis, and 54 patients (69%) had pain associated with calcinosis cutis. For 20 patients, the diagnosis was confirmed by skin biopsy; for 38 patients (49%), calcinosis cutis was confirmed using 1 or more imaging studies (radiography, computed tomography, magnetic resonance imaging, or ultrasonography).

Place holder to copy figure label and caption
Graphic Jump Location

Figure 1. A 58-year-old woman with classic dermatomyositis and extensive calcinosis cutis of the trunk (A) and extremities (B). The patient had associated ulcerations with focal extrusion of chalky granules.

Table Graphic Jump LocationTable 2. Anatomical Distribution of Calcinosis Cutis
TREATMENT OF CALCINOSIS CUTIS

Table 3 summarizes the treatment categories of the patients in the study and the best response to treatment that each patient achieved.

Table Graphic Jump LocationTable 3. Treatment Categories of 78 Patients Who Had Calcinosis Cutis Associated With ACTD
Specific Treatments

Calcium channel blockers were the most frequently used medical treatment; of 18 patients who received a calcium channel blocker, 17 received diltiazem (≤480 mg/d). Eight patients received colchicine (≤1.2 g/d), 6 each received intravenous immunoglobulin or minocycline hydrochloride (≤200 mg/d), 5 received bisphosphonates, and 4 were treated with warfarin sodium. Only 1 patient treated with medical therapy alone had a complete response: the patient received methotrexate (20 mg by mouth once weekly) combined with colchicine. Other treatments were given to 3 or fewer patients each and are reported in Table 4.

Table Graphic Jump LocationTable 4. Specific Treatment of 78 Patients With Calcinosis Cutis Associated With ACTD
Treatment Based on Calcinosis Cutis Severity

For a surrogate to judge the severity of calcinosis cutis, we enumerated the number of locations involved per patient, reasoning that more severely affected patients would have more calcinosis over more areas of their body. Patients were scored as having 1, 2, or 3 or more areas of the body affected (hands or feet, trunk, extremities, and head). We compared the number of body locations affected by calcinosis cutis with the number of calcinosis cutis treatments that each patient received by using a Kruskal-Wallis test (P = .07) (Figure 2).

Place holder to copy figure label and caption
Graphic Jump Location

Figure 2. Association between the number of calcinosis cutis locations and the number of calcinosis cutis treatments. The horizontal line in the middle of each box represents the median, and the bottom and top borders of the box mark the 25th and 75th percentiles, respectively. The points beyond these percentiles are outliers. The median and 75th percentiles were the same for 3 or more calcinosis cutis locations. P = .07.

Treatment Based on the Severity of the Underlying ACTD

For a surrogate measure of the severity of ACTD, we enumerated the number of treatments administered to each patient for their underlying ACTD, reasoning that the more treatments administered, the more severe the disease. We compared this treatment number with the number of treatments administered for calcinosis cutis and with the number of locations affected by calcinosis cutis (ie, 1, 2, or ≥3) (Figure 3). No significant relationship was present between the severity of the ACTD and the number of treatments administered for calcinosis cutis based on a Spearman rank correlation coefficient of 0.19 (P = .10). In addition, Figure 3 shows that no significant correlation existed between the severity of ACTD and the number of locations affected by calcinosis cutis based on the P value from a Kruskal-Wallis test (P = .24).

Place holder to copy figure label and caption
Graphic Jump Location

Figure 3. Association between the number of calcinosis cutis locations and the number of treatments for autoimmune connective tissue disease (ACTD). The horizontal line in the middle of each box represents the median, and the bottom and top borders of the box mark the 25th and 75th percentiles. The points beyond these percentiles are outliers. P = .24 by Kruskal-Wallis test.

Treatment With Warfarin

To investigate whether warfarin use may have affected the treatment response of the 19 patients who received medical therapy alone, we compared the best treatment result achieved in the 4 patients treated with warfarin for conditions other than calcinosis cutis while receiving treatment for calcinosis cutis with that in the 13 patients who did not receive warfarin during medical therapy for calcinosis cutis. There was no obvious difference in the response to treatment between these 2 groups: of those who received warfarin, 2 had a partial response, 1 had no response, and 1 had an unknown response, and of those who did not receive warfarin, 1 had a complete response, 3 had a partial response, 3 had no response, and 6 had an unknown response.

SURVIVAL

Three patients had no follow-up. For the other 75 patients, mean follow-up after diagnosis of calcinosis cutis was 104 months (median, 60 months; range, 1-696 months). Seven patients died, at a mean of 101 months after calcinosis cutis diagnosis (median, 120 months; range, 3-228 months). Cause of death was metastatic breast carcinoma and adenocarcinoma of unknown primary in 2 patients and unknown in the other 5. Among the 68 patients who were still alive at the last follow-up, the mean duration of follow-up was 104 months (median, 58 months; range, 1-696 months).

Overall survival was 96% (95% CI, 91%-100%; still at risk, n = 38) at 60 months, 91% (95% CI, 82%-100%; still at risk, n = 22) at 120 months, 87% (95% CI, 75%-100%; still at risk, n = 14) at 180 months, and 72% (95% CI, 54%-97%; still at risk, n = 9) at 240 months. The overall survival rate for patients in this study was not significantly different from the expected survival rate for age- and sex-matched Minnesota residents (P = .12).

The clinical features of calcinosis cutis have been reported to differ on the basis of the underlying ACTD with which the calcinosis cutis is associated.1,6 The present findings corroborate this observation. We discuss briefly the present findings and what has been reported in the medical literature previously. Reiter et al6,7 recently reviewed the diagnostic pathway and treatment options for calcinosis cutis.

UNDERLYING ACTD
Systemic Sclerosis

Calcinosis cutis has been reported to most frequently occur 10 to 12 years after the onset of systemic sclerosis.1,8 The present results suggest that the mean time to the onset of calcinosis cutis after diagnosis of systemic sclerosis is 7.5 years. Investigators1 have reported that the most frequently involved body site of calcinosis cutis in systemic sclerosis is the hands and feet, particularly the fingers; the present findings concur with these reports.

Dermatomyositis

Calcinosis cutis has been reported to be more common in juvenile- vs adult-onset dermatomyositis (44%-70% vs 20%).1 We observed that the onset of calcinosis cutis (after the diagnosis of dermatomyositis) in juvenile dermatomyositis was much earlier than in classic dermatomyositis (2.9 years vs 7.8 years), which agrees with previous studies.1 We also found that in juvenile and classic dermatomyositis, the location of the calcinosis tended to involve the extremities, a finding that agrees with previous studies.9 Involvement of the head, although rare, was much more likely in juvenile dermatomyositis than in any other ACTD.

Systemic Lupus Erythematosus and Lupus Panniculitis

Rothe et al10 reviewed 23 previously described cases of calcinosis cutis associated with systemic lupus erythematosus (SLE) and remarked that the disease was clinically silent in many of these patients. Of the 78 patients in the present case series, we observed that only 2 had calcinosis cutis and an underlying diagnosis of SLE. The time to diagnosis of calcinosis cutis has been reported to occur after long-standing systemic disease.10 We confirmed this finding because the mean time to diagnosis of calcinosis cutis in the 2 patients was more than 20 years after the diagnosis of SLE. Lupus panniculitis occurs in 2% to 3% of patients with SLE,11 and calcinosis cutis has been reported to occur in association with it.1,11 The present case series also had 4 patients with lupus panniculitis. The mean time between the diagnosis of ACTD and the onset of calcinosis cutis was much shorter in lupus panniculitis (4.8 years) than in SLE (21.5 years).

Overlap CTD

Overlap CTD rarely has been reported in association with calcinosis cutis. Chan et al12 described 2 patients with overlap CTD (1 with dermatomyositis and SLE overlap and the other with systemic sclerosis and SLE overlap) who both had calcinosis cutis on their left buttock 5 and 3 years after presentation of their underlying ACTDs. We describe 6 patients with overlap CTD and calcinosis cutis. Given the small size of this patient population and the heterogeneous presentations of the ACTD, it is difficult to draw conclusions about the clinical behavior of calcinosis cutis in overlap CTD.

Undifferentiated CTD

Calcinosis cutis has been reported rarely as being associated with underlying undifferentiated CTD. Herein, we describe 6 such patients. Torralba et al13 described a patient who 4 years after diagnosis of undifferentiated CTD had calcinosis involving the upper and lower extremities and the submandibular areas.

Mixed CTD

We found only 4 patients with mixed CTD and calcinosis cutis. The location of the calcinosis cutis differed. There have been rare reports of dystrophic calcinosis cutis associated with underlying mixed CTD.14,15 Itoh et al14 described 1 patient with dystrophic calcinosis and mixed CTD. In this patient, the onset of calcinosis occurred only 3 months after the diagnosis of mixed CTD. The calcinosis diffusely involved the legs and buttocks. The patient died of pulmonary fibrosis, thought to be a sequela of the CTD.

Polymyositis and Rheumatoid Arthritis

We describe calcinosis cutis in 1 patient with polymyositis and 1 patient with rheumatoid arthritis. In both patients, calcinosis cutis involved the extremities alone. Rarely, polymyositis has been described in association with calcinosis cutis.16,17 More recently, a case was reported of dystrophic calcinosis cutis of the buttocks and elbow in a patient with rheumatoid arthritis.18

TREATMENTS

We discuss the most frequently used and most efficacious treatments in this case series, and we discuss the findings and compare them with those in the literature.

Calcium Channel Blockers

The mechanism by which this class of medications treats calcinosis cutis is unclear. It has been suggested to occur through a decrease in the influx of calcium ions into cells and, thus, correction of an abnormal imbalance of intracellular calcium concentration that may lead to crystal formation.19 Calcium channel blockers were the most frequently used medical treatment for calcinosis cutis in the present study. Of the medical therapies, this class of medications was the most efficacious, with 10 of the 18 patients responding favorably to treatment and showing improvement in their cutaneous lesions. Only 5 patients did not respond to treatment or their cutaneous lesions worsened.

Colchicine

Colchicine has been reported to have positive effects in reducing calcinosis20,21 and to have no effect on calcinosis but rather on inflammation secondary to calcinosis.20,22 In the present case series, 3 of 8 patients treated with colchicine responded favorably, with 1 patient having a complete response (this was the only patient treated with medical therapy alone who had a complete response).

Minocycline

Robertson et al23 described a series of 9 patients with systemic sclerosis and calcinosis cutis who were treated with low-dose minocycline. Of the 9 patients, 8 were reported to achieve improvement in their calcinosis, as measured through clinical examination and radiologic studies. The mechanism by which minocycline treats calcinosis cutis is unknown; however, investigators23,24 have postulated that it is a combination of anti-inflammatory effects, inhibition of collagenolytic enzymes (particularly, matrix metalloproteinase), and chelation of calcium. It is unclear why patients in the present case series did not respond as favorably to this treatment as previously reported. Of note, we did not monitor response using imaging studies; rather, the responses that we could abstract were those described clinically in the patient's medical record. This detail may explain the discrepancy between the present retrospective review and the prospective trial of Robertson et al.23

Intravenous Immunoglobulin

Intravenous immunoglobulin has been tried as a therapy for dystrophic calcinosis cutis, with positive25,26 and negative27 results. When intravenous immunoglobulin has worked, investigators25 have postulated that its effectiveness occurs through decreased inflammation, possibly through inhibition of macrophage function. In the present series, 6 patients received treatment with intravenous immunoglobulin; however, the results of the treatment in all 6 patients were unclear because of either the lack of follow-up data or incomplete information in the medical records.

Bisphosphonates

Bisphosphonates inhibit calcium turnover and, thus, have been tried as therapies for calcinosis cutis. Their use has been investigated for a long time, with positive28 and negative29 results. One case of calcinosis cutis in the clinical setting of juvenile dermatomyositis showed improvement with alendronate therapy despite preceding failure with probenecid and diltiazem.30 In the present case series, 5 patients received treatment with this class of medications. Only 1 patient had a partial response, and 3 had no response (1 response was unknown).

Warfarin

Lesions of calcinosis cutis have been found to contain elevated levels of γ-carboxyglutamic acid.31 Carboxylated glutamine can bind calcium and, thus, was postulated to be part of a mechanism promoting cutaneous calcification.32 Because the generation of γ-carboxyglutamic acid is vitamin K dependent, warfarin was suggested as a possible treatment option for calcinosis cutis through its inhibition of γ-carboxyglutamic acid generation.32 Since the study by Berger et al,32 there have been conflicting reports about the efficacy of warfarin therapy for calcinosis cutis. These conflicting data have led to the hypothesis that the response of calcinosis cutis to warfarin treatment depends on the size of the lesions and the time lapse since lesion formation, with larger and older lesions being resistant to the treatment.33

In the present case series, 4 patients were treated with warfarin directly for their calcinosis cutis. Among them, only 1 patient partially responded to treatment. Of the patients receiving medical therapy alone, an additional 4 had received warfarin. The best response to treatment achieved for calcinosis cutis in this patient set did not differ from that of patients who never received warfarin for any reason.

Surgical Excision

Minami et al34 described widespread calcinosis cutis in 2 patients with SLE. Surgical excision was used to remove the calcification of the forearm in these patients because of the pain elicited in that region. In both patients, calcification did not return to the excised areas. In 2 separate patients, Saddic et al35 and Wu and Metz36 reported excellent results from incision and drainage of painful calcific lesions on the fingers of patients with underlying rheumatic disease. Bogoch and Gross,37 in a review of 34 studies describing hand surgery in patients with systemic sclerosis, found that 13 of these reports were for treatment of calcinosis cutis. Most of the studies reviewed were reported to have resulted in “relief of pain” and “improved function.” Risks were noted of slower wound healing and a possible reduction in range of motion.

In the present study, 11 patients received surgical excision alone, and all 11 responded, with 8 having a complete response. In cases with either discrete calcification or widespread calcification with discrete symptomatic lesions, surgical excision of these areas may provide benefit for patients.

Treatment of Calcinosis Cutis Based on Underlying ACTD

We could not determine whether a specific calcinosis cutis treatment benefitted patients on the basis of their underlying ACTD. There did not seem to be a predilection for a treatment type based on the underlying ACTD.

CALCINOSIS CUTIS SEVERITY NOT PREDICTED BY ACTD SEVERITY

Some investigators5,38 have suggested that the severity of calcinosis cutis in the clinical setting of underlying ACTD is related to the severity of the underlying ACTD and the duration of disease activity. We examined this hypothesis using a surrogate marker for disease severity—the number of treatments used. We asked whether a greater number of treatments used for the underlying ACTD correlated with worse calcinosis cutis. Using this evaluation method, we did not detect a significant correlation.

RECOMMENDATIONS

On the basis of the results of the present study, we propose an approach to managing calcinosis cutis in the clinical setting of ACTD, as summarized in Table 5. Reiter et al7 recently reviewed additional treatment options for calcinosis cutis that were either not beneficial or not used in the present cohort of 78 patients; these additional treatment options include warfarin (1 mg/d), bisphosphonates (eg, alendronate [10 mg/d]), minocycline (50-100 mg/d), ceftriaxone (2 g/d for 20 days), aluminum hydroxide (1.8-2.4 g/d), probenecid (1.5 g/d), intravenous immunoglobulin (2 g/kg/mo), intralesional corticosteroids, extracorporeal shock wave lithotripsy, and carbon dioxide laser.

Table Graphic Jump LocationTable 5. Recommendations for the Management of Calcinosis Cutis Associated With ACTD Based on the Findings From the Present Study
CONCLUSIONS

We report a case series of 78 patients with calcinosis cutis occurring in association with underlying ACTD. We acknowledge the study's limitations: its retrospective design, lack of certain clinical data for some patients, inability to determine in all patients whether the ACTD was active at the time of calcinosis onset, and incomplete follow-up for some patients. The study design did not allow us to determine whether the sex distribution of calcinosis cutis observed was different from the sex distribution of the underlying ACTDs. Moreover, this study was not population based and, therefore, could not determine the incidence and prevalence of calcinosis cutis in each particular ACTD.

Nonetheless, clinical features of calcinosis cutis in this study differed on the basis of underlying disease. Thus, this study may help guide physicians in the education of their patients' expectations for the development of lesions over time as the respective ACTD progresses. We recommend that surgical excision be considered for patients with discrete lesions or particularly symptomatic lesions. In patients for whom surgical excision was contraindicated and medical therapy was desired, the best results were achieved with diltiazem therapy, although reproducibility from patient to patient was variable in this study. Prospective controlled trials are needed to further determine whether specific treatments for calcinosis cutis are more effective for patients with certain ACTDs, thus allowing therapeutic measures to be tailored rationally to each patient depending on his or her underlying ACTD.

Correspondence: David A. Wetter, MD, Department of Dermatology, Mayo Clinic, 200 First St SW, Rochester, MN 55905 (wetter.david@mayo.edu).

Accepted for Publication: October 6, 2011.

Published Online: December 19, 2011. doi:10.1001/archdermatol.2011.2052

Author Contributions: All authors had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: Balin, Wetter, and Davis. Acquisition of data: Balin, Wetter, and Andersen. Analysis and interpretation of data: Balin, Wetter, and Davis. Drafting of the manuscript: Balin and Wetter. Critical revision of the manuscript for important intellectual content: Balin, Wetter, Andersen, and Davis. Administrative, technical, and material support: Balin. Study supervision: Wetter and Davis.

Financial Disclosure: None reported.

Additional Contributions: Christine M. Lohse, MS, assisted with the statistical analysis of the data.

Walsh JS, Fairley JA. Calcifying disorders of the skin.  J Am Acad Dermatol. 1995;33(5, pt 1):693-710
PubMed   |  Link to Article
Touart DM, Sau P. Cutaneous deposition diseases: part II.  J Am Acad Dermatol. 1998;39(4, pt 1):527-546
PubMed   |  Link to Article
Dutz J. Treatment options for the cutaneous manifestations of systemic sclerosis.  Skin Therapy Lett. 2000;6(1):3-5
PubMed
Boulman N, Slobodin G, Rozenbaum M, Rosner I. Calcinosis in rheumatic diseases.  Semin Arthritis Rheum. 2005;34(6):805-812
PubMed   |  Link to Article
James WD, Berger TG, Elston DM. Connective tissue diseases. In: James WD, Berger TG, Elston DM, eds. Andrews' Diseases of the Skin: Clinical Dermatology. 11th ed. London, UK: Saunders Elsevier; 2011:155-181
Reiter N, El-Shabrawi L, Leinweber B, Berghold A, Aberer E. Calcinosis cutis, part I: diagnostic pathway.  J Am Acad Dermatol. 2011;65(1):1-14
PubMed   |  Link to Article
Reiter N, El-Shabrawi L, Leinweber B, Berghold A, Aberer E. Calcinosis cutis, part II: treatment options.  J Am Acad Dermatol. 2011;65(1):15-24
PubMed   |  Link to Article
Raimer S. Calcinosis cutis.  Curr Concepts Skin Dis. 1985;6:9-15
Blane CE, White SJ, Braunstein EM, Bowyer SL, Sullivan DB. Patterns of calcification in childhood dermatomyositis.  AJR Am J Roentgenol. 1984;142(2):397-400
PubMed
Rothe MJ, Grant-Kels JM, Rothfield NF. Extensive calcinosis cutis with systemic lupus erythematosus.  Arch Dermatol. 1990;126(8):1060-1063
PubMed   |  Link to Article
Winkelmann RK. Panniculitis in connective tissue disease.  Arch Dermatol. 1983;119(4):336-344
PubMed   |  Link to Article
Chan AT, Wordsworth BP, McNally J. Overlap connective tissue disease, pulmonary fibrosis, and extensive subcutaneous calcification.  Ann Rheum Dis. 2003;62(7):690-691
PubMed   |  Link to Article
Torralba TP, Li-Yu J, Navarra ST. Successful use of diltiazem in calcinosis caused by connective tissue disease.  J Clin Rheumatol. 1999;5(2):74-78
PubMed   |  Link to Article
Itoh O, Nishimaki T, Itoh M,  et al.  Mixed connective tissue disease with severe pulmonary hypertension and extensive subcutaneous calcification.  Intern Med. 1998;37(4):421-425
PubMed   |  Link to Article
Bäurle G, Hornstein OP. Generalized cutaneous calcinosis and mixed connective tissue disease.  Dermatologica. 1979;158(4):257-268
PubMed   |  Link to Article
Arlet J, Dalous A, Degoy A, Salanova J, Limouzy P. Polymyositis with diffuse calcinosis (universal calcinosis): apropos of 2 cases in children [in French].  Rev Rhum Mal Osteoartic. 1965;32(10):593-599
PubMed
Lucas D. Polymyositis with universal calcinosis [in German].  Arch Kinderheilkd. 1971;183(4):359-369
PubMed
Harigane K, Mochida Y, Ishii K, Ono S, Mitsugi N, Saito T. Dystrophic calcinosis in a patient with rheumatoid arthritis.  Mod Rheumatol. 2011;21(1):85-88
PubMed   |  Link to Article
Ichiki Y, Akiyama T, Shimozawa N, Suzuki Y, Kondo N, Kitajima Y. An extremely severe case of cutaneous calcinosis with juvenile dermatomyositis, and successful treatment with diltiazem.  Br J Dermatol. 2001;144(4):894-897
PubMed   |  Link to Article
Fuchs D, Fruchter L, Fishel B, Holtzman M, Yaron M. Colchicine suppression of local inflammation due to calcinosis in dermatomyositis and progressive systemic sclerosis.  Clin Rheumatol. 1986;5(4):527-530
PubMed
Vereecken P, Stallenberg B, Tas S, de Dobbeleer G, Heenen M. Ulcerated dystrophic calcinosis cutis secondary to localised linear scleroderma.  Int J Clin Pract. 1998;52(8):593-594
PubMed
Taborn J, Bole GG, Thompson GR. Colchicine suppression of local and systemic inflammation due to calcinosis universalis in chronic dermatomyositis.  Ann Intern Med. 1978;89(5, pt 1):648-649
PubMed
Robertson LP, Marshall RW, Hickling P. Treatment of cutaneous calcinosis in limited systemic sclerosis with minocycline.  Ann Rheum Dis. 2003;62(3):267-269
PubMed   |  Link to Article
Cohen H, Solomon V, Alferiev IS,  et al.  Bisphosphonates and tetracycline: experimental models for their evaluation in calcium-related disorders.  Pharm Res. 1998;15(4):606-613
PubMed   |  Link to Article
Schanz S, Ulmer A, Fierlbeck G. Response of dystrophic calcification to intravenous immunoglobulin.  Arch Dermatol. 2008;144(5):585-587
PubMed   |  Link to Article
Peñate Y, Guillermo N, Melwani P, Martel R, Hernández-Machín B, Borrego L. Calcinosis cutis associated with amyopathic dermatomyositis: response to intravenous immunoglobulin.  J Am Acad Dermatol. 2009;60(6):1076-1077
PubMed   |  Link to Article
Kalajian AH, Perryman JH, Callen JP. Intravenous immunoglobulin therapy for dystrophic calcinosis cutis: unreliable in our hands.  Arch Dermatol. 2009;145(3):334-335
PubMed   |  Link to Article
Mukamel M, Horev G, Mimouni M. New insight into calcinosis of juvenile dermatomyositis: a study of composition and treatment.  J Pediatr. 2001;138(5):763-766
PubMed   |  Link to Article
Metzger AL, Singer FR, Bluestone R, Pearson CM. Failure of disodium etidronate in calcinosis due to dermatomyositis and scleroderma.  N Engl J Med. 1974;291(24):1294-1296
PubMed   |  Link to Article
Ambler GR, Chaitow J, Rogers M, McDonald DW, Ouvrier RA. Rapid improvement of calcinosis in juvenile dermatomyositis with alendronate therapy.  J Rheumatol. 2005;32(9):1837-1839
PubMed
Lian JB, Skinner M, Glimcher MJ, Gallop P. The presence of γ-carboxyglutamic acid in the proteins associated with ectopic calcification.  Biochem Biophys Res Commun. 1976;73(2):349-355
PubMed   |  Link to Article
Berger RG, Featherstone GL, Raasch RH, McCartney WH, Hadler NM. Treatment of calcinosis universalis with low-dose warfarin.  Am J Med. 1987;83(1):72-76
PubMed   |  Link to Article
Cukierman T, Elinav E, Korem M, Chajek-Shaul T. Low dose warfarin treatment for calcinosis in patients with systemic sclerosis.  Ann Rheum Dis. 2004;63(10):1341-1343
PubMed   |  Link to Article
Minami A, Suda K, Kaneda K, Kumakiri M. Extensive subcutaneous calcification of the forearm in systemic lupus erythematosus.  J Hand Surg Br. 1994;19(5):638-641
PubMed   |  Link to Article
Saddic N, Miller JJ, Miller OF III, Clarke JT. Surgical debridement of painful fingertip calcinosis cutis in CREST syndrome.  Arch Dermatol. 2009;145(2):212-213
PubMed   |  Link to Article
Wu JJ, Metz BJ. Calcinosis cutis of juvenile dermatomyositis treated with incision and drainage.  Dermatol Surg. 2008;34(4):575-577
PubMed   |  Link to Article
Bogoch ER, Gross DK. Surgery of the hand in patients with systemic sclerosis: outcomes and considerations.  J Rheumatol. 2005;32(4):642-648
PubMed
Fisler RE, Liang MG, Fuhlbrigge RC, Yalcindag A, Sundel RP. Aggressive management of juvenile dermatomyositis results in improved outcome and decreased incidence of calcinosis.  J Am Acad Dermatol. 2002;47(4):505-511
PubMed   |  Link to Article

Figures

Place holder to copy figure label and caption
Graphic Jump Location

Figure 1. A 58-year-old woman with classic dermatomyositis and extensive calcinosis cutis of the trunk (A) and extremities (B). The patient had associated ulcerations with focal extrusion of chalky granules.

Place holder to copy figure label and caption
Graphic Jump Location

Figure 2. Association between the number of calcinosis cutis locations and the number of calcinosis cutis treatments. The horizontal line in the middle of each box represents the median, and the bottom and top borders of the box mark the 25th and 75th percentiles, respectively. The points beyond these percentiles are outliers. The median and 75th percentiles were the same for 3 or more calcinosis cutis locations. P = .07.

Place holder to copy figure label and caption
Graphic Jump Location

Figure 3. Association between the number of calcinosis cutis locations and the number of treatments for autoimmune connective tissue disease (ACTD). The horizontal line in the middle of each box represents the median, and the bottom and top borders of the box mark the 25th and 75th percentiles. The points beyond these percentiles are outliers. P = .24 by Kruskal-Wallis test.

Tables

Table Graphic Jump LocationTable 1. Characteristics and Prevalence of ACTD Associated With Calcinosis Cutis
Table Graphic Jump LocationTable 2. Anatomical Distribution of Calcinosis Cutis
Table Graphic Jump LocationTable 3. Treatment Categories of 78 Patients Who Had Calcinosis Cutis Associated With ACTD
Table Graphic Jump LocationTable 4. Specific Treatment of 78 Patients With Calcinosis Cutis Associated With ACTD
Table Graphic Jump LocationTable 5. Recommendations for the Management of Calcinosis Cutis Associated With ACTD Based on the Findings From the Present Study

References

Walsh JS, Fairley JA. Calcifying disorders of the skin.  J Am Acad Dermatol. 1995;33(5, pt 1):693-710
PubMed   |  Link to Article
Touart DM, Sau P. Cutaneous deposition diseases: part II.  J Am Acad Dermatol. 1998;39(4, pt 1):527-546
PubMed   |  Link to Article
Dutz J. Treatment options for the cutaneous manifestations of systemic sclerosis.  Skin Therapy Lett. 2000;6(1):3-5
PubMed
Boulman N, Slobodin G, Rozenbaum M, Rosner I. Calcinosis in rheumatic diseases.  Semin Arthritis Rheum. 2005;34(6):805-812
PubMed   |  Link to Article
James WD, Berger TG, Elston DM. Connective tissue diseases. In: James WD, Berger TG, Elston DM, eds. Andrews' Diseases of the Skin: Clinical Dermatology. 11th ed. London, UK: Saunders Elsevier; 2011:155-181
Reiter N, El-Shabrawi L, Leinweber B, Berghold A, Aberer E. Calcinosis cutis, part I: diagnostic pathway.  J Am Acad Dermatol. 2011;65(1):1-14
PubMed   |  Link to Article
Reiter N, El-Shabrawi L, Leinweber B, Berghold A, Aberer E. Calcinosis cutis, part II: treatment options.  J Am Acad Dermatol. 2011;65(1):15-24
PubMed   |  Link to Article
Raimer S. Calcinosis cutis.  Curr Concepts Skin Dis. 1985;6:9-15
Blane CE, White SJ, Braunstein EM, Bowyer SL, Sullivan DB. Patterns of calcification in childhood dermatomyositis.  AJR Am J Roentgenol. 1984;142(2):397-400
PubMed
Rothe MJ, Grant-Kels JM, Rothfield NF. Extensive calcinosis cutis with systemic lupus erythematosus.  Arch Dermatol. 1990;126(8):1060-1063
PubMed   |  Link to Article
Winkelmann RK. Panniculitis in connective tissue disease.  Arch Dermatol. 1983;119(4):336-344
PubMed   |  Link to Article
Chan AT, Wordsworth BP, McNally J. Overlap connective tissue disease, pulmonary fibrosis, and extensive subcutaneous calcification.  Ann Rheum Dis. 2003;62(7):690-691
PubMed   |  Link to Article
Torralba TP, Li-Yu J, Navarra ST. Successful use of diltiazem in calcinosis caused by connective tissue disease.  J Clin Rheumatol. 1999;5(2):74-78
PubMed   |  Link to Article
Itoh O, Nishimaki T, Itoh M,  et al.  Mixed connective tissue disease with severe pulmonary hypertension and extensive subcutaneous calcification.  Intern Med. 1998;37(4):421-425
PubMed   |  Link to Article
Bäurle G, Hornstein OP. Generalized cutaneous calcinosis and mixed connective tissue disease.  Dermatologica. 1979;158(4):257-268
PubMed   |  Link to Article
Arlet J, Dalous A, Degoy A, Salanova J, Limouzy P. Polymyositis with diffuse calcinosis (universal calcinosis): apropos of 2 cases in children [in French].  Rev Rhum Mal Osteoartic. 1965;32(10):593-599
PubMed
Lucas D. Polymyositis with universal calcinosis [in German].  Arch Kinderheilkd. 1971;183(4):359-369
PubMed
Harigane K, Mochida Y, Ishii K, Ono S, Mitsugi N, Saito T. Dystrophic calcinosis in a patient with rheumatoid arthritis.  Mod Rheumatol. 2011;21(1):85-88
PubMed   |  Link to Article
Ichiki Y, Akiyama T, Shimozawa N, Suzuki Y, Kondo N, Kitajima Y. An extremely severe case of cutaneous calcinosis with juvenile dermatomyositis, and successful treatment with diltiazem.  Br J Dermatol. 2001;144(4):894-897
PubMed   |  Link to Article
Fuchs D, Fruchter L, Fishel B, Holtzman M, Yaron M. Colchicine suppression of local inflammation due to calcinosis in dermatomyositis and progressive systemic sclerosis.  Clin Rheumatol. 1986;5(4):527-530
PubMed
Vereecken P, Stallenberg B, Tas S, de Dobbeleer G, Heenen M. Ulcerated dystrophic calcinosis cutis secondary to localised linear scleroderma.  Int J Clin Pract. 1998;52(8):593-594
PubMed
Taborn J, Bole GG, Thompson GR. Colchicine suppression of local and systemic inflammation due to calcinosis universalis in chronic dermatomyositis.  Ann Intern Med. 1978;89(5, pt 1):648-649
PubMed
Robertson LP, Marshall RW, Hickling P. Treatment of cutaneous calcinosis in limited systemic sclerosis with minocycline.  Ann Rheum Dis. 2003;62(3):267-269
PubMed   |  Link to Article
Cohen H, Solomon V, Alferiev IS,  et al.  Bisphosphonates and tetracycline: experimental models for their evaluation in calcium-related disorders.  Pharm Res. 1998;15(4):606-613
PubMed   |  Link to Article
Schanz S, Ulmer A, Fierlbeck G. Response of dystrophic calcification to intravenous immunoglobulin.  Arch Dermatol. 2008;144(5):585-587
PubMed   |  Link to Article
Peñate Y, Guillermo N, Melwani P, Martel R, Hernández-Machín B, Borrego L. Calcinosis cutis associated with amyopathic dermatomyositis: response to intravenous immunoglobulin.  J Am Acad Dermatol. 2009;60(6):1076-1077
PubMed   |  Link to Article
Kalajian AH, Perryman JH, Callen JP. Intravenous immunoglobulin therapy for dystrophic calcinosis cutis: unreliable in our hands.  Arch Dermatol. 2009;145(3):334-335
PubMed   |  Link to Article
Mukamel M, Horev G, Mimouni M. New insight into calcinosis of juvenile dermatomyositis: a study of composition and treatment.  J Pediatr. 2001;138(5):763-766
PubMed   |  Link to Article
Metzger AL, Singer FR, Bluestone R, Pearson CM. Failure of disodium etidronate in calcinosis due to dermatomyositis and scleroderma.  N Engl J Med. 1974;291(24):1294-1296
PubMed   |  Link to Article
Ambler GR, Chaitow J, Rogers M, McDonald DW, Ouvrier RA. Rapid improvement of calcinosis in juvenile dermatomyositis with alendronate therapy.  J Rheumatol. 2005;32(9):1837-1839
PubMed
Lian JB, Skinner M, Glimcher MJ, Gallop P. The presence of γ-carboxyglutamic acid in the proteins associated with ectopic calcification.  Biochem Biophys Res Commun. 1976;73(2):349-355
PubMed   |  Link to Article
Berger RG, Featherstone GL, Raasch RH, McCartney WH, Hadler NM. Treatment of calcinosis universalis with low-dose warfarin.  Am J Med. 1987;83(1):72-76
PubMed   |  Link to Article
Cukierman T, Elinav E, Korem M, Chajek-Shaul T. Low dose warfarin treatment for calcinosis in patients with systemic sclerosis.  Ann Rheum Dis. 2004;63(10):1341-1343
PubMed   |  Link to Article
Minami A, Suda K, Kaneda K, Kumakiri M. Extensive subcutaneous calcification of the forearm in systemic lupus erythematosus.  J Hand Surg Br. 1994;19(5):638-641
PubMed   |  Link to Article
Saddic N, Miller JJ, Miller OF III, Clarke JT. Surgical debridement of painful fingertip calcinosis cutis in CREST syndrome.  Arch Dermatol. 2009;145(2):212-213
PubMed   |  Link to Article
Wu JJ, Metz BJ. Calcinosis cutis of juvenile dermatomyositis treated with incision and drainage.  Dermatol Surg. 2008;34(4):575-577
PubMed   |  Link to Article
Bogoch ER, Gross DK. Surgery of the hand in patients with systemic sclerosis: outcomes and considerations.  J Rheumatol. 2005;32(4):642-648
PubMed
Fisler RE, Liang MG, Fuhlbrigge RC, Yalcindag A, Sundel RP. Aggressive management of juvenile dermatomyositis results in improved outcome and decreased incidence of calcinosis.  J Am Acad Dermatol. 2002;47(4):505-511
PubMed   |  Link to Article

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