Journals / European Journal of Rheumatology / 2014 / Cilt: 1 - Sayı: 4

Chondrodermatitis nodularis chronica helicis in a patient with systemic sclerosis associated with primary biliary cirrhosis (Reynolds syndrome): A case report

Pages
161–163
Publication Date
2022-11-05
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Although this condition is infrequent, it is necessary to know, because it may occur in patients with systemic sclerosis and be mistaken for neoplasms, such as basal cell and squamous cell carcinoma, and these patients have an increased risk for the development of skin malignancies

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Chondrodermatitis nodularis chronica helicis is a rare non-neoplastic inflammatory and degenerative process of the external ear, characterized by necrobiotic changes in the dermis that extend down to the perichondrium.
📊
Key Findings & Data:We report a 70-year-old woman diagnosed with primary biliary cirrhosis at age 47 and with limited cutaneous systemic sclerosis at age 54 who developed a painful ulcerated nodule on the helical rim of the left ear shortly after the last diagnosis.
💡
Conclusion & Impact:Although this condition is infrequent, it is necessary to know, because it may occur in patients with systemic sclerosis and be mistaken for neoplasms, such as basal cell and squamous cell carcinoma, and these patients have an increased risk for the development of skin malignancies
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Chondrodermatitis nodularis chronica helicis is a rare non-neoplastic inflammatory and degenerative process of the external ear, characterized by necrobiotic changes in the dermis that extend down to the perichondrium. This condition has been occasionally reported in patients with limited cutaneous systemic sclerosis but not in those with concomitant primary biliary cirrhosis; this association is known as Reynolds syndrome. We report a 70-year-old woman diagnosed with primary biliary cirrhosis at age 47 and with limited cutaneous systemic sclerosis at age 54 who developed a painful ulcerated nodule on the helical rim of the left ear shortly after the last diagnosis. The lesion was excised because of the suspicion of malignancy, but the histopathology was consistent with chondrodermatitis nodularis chronica helicis. Although this condition is infrequent, it is necessary to know, because it may occur in patients with systemic sclerosis and be mistaken for neoplasms, such as basal cell and squamous cell carcinoma, and these patients have an increased risk for the development of skin malignancies

🔖

Cite This Article

GİRALDO, W. A. S., GARCIA, C. G., ALONSO, E. D. L. H., BUJIDOS, C. D. L. P. (2022). Chondrodermatitis nodularis chronica helicis in a patient with systemic sclerosis associated with primary biliary cirrhosis (Reynolds syndrome): A case report. European Journal of Rheumatology, Cilt: 1 - Sayı: 4, 161–163. https://ajindex.com/articles/650451

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (3)

  1. Varga J. Etiology and pathogenesis of Sclero- derma. In: Firestein GS, Budd RC, Gabriel SE, McInnes IB, O'Dell JR, editors. Kelley's Textbook of Rheumatology. 9th ed. Philadelphia: Saun- ders - Elsevier; 2013. p. 1343-1365. [CrossRef] Koulaouzidis A, Bhat S, Moschos J. Skin mani- festations of liver diseases. Ann Hepatol 2007; 6: 181-4.
  2. Reynolds TB, Denison EK, Frankl HD, Lieberman FL, Peters RL. Primary biliary cirrhosis with scle- roderma, Raynaud's phenomenon and telang- iectasia. New syndrome. Am J Med 1971; 50: 302-12. [CrossRef] Thompson LD. Chondrodermatitis nodularis 9. Upile T, Patel NN, Jerjes W, Singh NU, Sandison helicis. Ear Nose Throat J 2007; 86: 734-5.
  3. Bottomley WW, Goodfield MD. Chondroderma- titis nodularis helicis occurring with systemic sclerosis-an under-reported association? Clin Exp Dermatol 1994; 19: 219-20. [CrossRef] Newcomer VD, Steffen CG, Sternberg TH, Lichtenstein L. Chondrodermatitis nodularis chronica helicis; report of ninety-four cases and survey of literature, with emphasis upon patho- genesis and treatment. AMA Arch Derm Syphi- lol 1953; 68: 241-55. [CrossRef] Wagner G, Liefeith J, Sachse MM. Clinical ap- pearance, differential diagnoses and therapeu- tical options of chondrodermatitis nodularis chronica helicis Winkler. J Dtsch Dermatol Ges 2011; 9: 287-91. [CrossRef] Sasaki T, Nishizawa H, Sugita Y. Chondroderma- titis nodularis helicis in childhood dermatomy- ositis. Br J Dermatol 1999; 141: 363-5. [CrossRef] A, Michaels L. Advances in the understanding of chondrodermatitis nodularis chronica hel- ices: the perichondrial vasculitis theory. Clin Otolaryngol 2009; 34: 147-50. [CrossRef] Yoshinaga E, Enomoto U, Fujimoto N, Ohnishi Y, Tajima S, Ishibashi A. A case of chondroderma- titis nodularis chronica helicis with an autoanti- body to denatured type II collagen. Acta Derm Venereol 2001; 81: 137-8. [CrossRef]