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Erschienen in: Clinical Rheumatology 12/2019

12.08.2019 | Original Article

Analysis of the clinical characteristics of thirteen patients with Weber-Christian panniculitis

verfasst von: Wei Zheng, Wenyuan Song, Qingqing Wu, Qiaoqiao Yin, Chaolan Pan, Hongying Pan

Erschienen in: Clinical Rheumatology | Ausgabe 12/2019

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Abstract

Background

Weber-Christian disease (WCD) is an uncommon, idiopathic disease that is challenging to diagnose and has an unclear treatment protocol. We reviewed thirteen patients with WCD and analyzed their clinical characteristics. The purpose of this article was to improve the understanding of this rare disorder.

Methods

Thirteen cases of WCD were analyzed retrospectively regarding their clinical manifestation, laboratory results, misdiagnoses, therapy, and outcome.

Results

Of the thirteen patients diagnosed with WCD, the majority were female (male to female ratio, 2:11), with a mean patient age of 50.1 years. Subcutaneous nodules were the most commonly reported symptom, followed by fever, arthralgias/arthritis, and myalgia. The laboratory results were typically nonspecific. In total, 61.5% patients were misdiagnosed before pathology confirmed the diagnosis of WCD. Most patients were treated with corticosteroids and/or immunosuppressants. Two patients were treated surgically. While long-term remission was successfully achieved in some patients, others had recurrent symptoms.

Conclusion

WCD was predominantly observed in female patients in our cohort. Subcutaneous nodules and fever were the most common clinical characteristics. In addition, the patients’ laboratory test results were nonspecific, which led to a high misdiagnosis rate. In this study population, corticosteroid and/or immunosuppressant treatments were efficacious therapeutic interventions for WCD.
Key Points
Subcutaneous nodules and fever were the most common clinical characteristics in Weber-Christian panniculitis.
Misdiagnosis rate was higher in Weber-Christian panniculitis patient; tumors, bacterial infections and rheumatic diseases were the most common misdiagnoses.
Corticosteroid and/or immunosuppressant therapy was effective in most Weber-Christian panniculitis patients.
Literatur
2.
Zurück zum Zitat Weber FP (1925) A case of relapsing nonsuppurative pannicultis showing phagocytosis of subcutaneous fat cells by macrophages. Br J Dermatol 37:301–311CrossRef Weber FP (1925) A case of relapsing nonsuppurative pannicultis showing phagocytosis of subcutaneous fat cells by macrophages. Br J Dermatol 37:301–311CrossRef
3.
Zurück zum Zitat Christian HA (1928) Relapsing febrile nodular nonsuppurative panniculitis. Arch Intern Med 42:338–351CrossRef Christian HA (1928) Relapsing febrile nodular nonsuppurative panniculitis. Arch Intern Med 42:338–351CrossRef
4.
Zurück zum Zitat Bailey RJ (1937) Relapsing febrile nodular nonsuppurative panniculitis (Weber-Christian disease). JAMA 109:1419–1425CrossRef Bailey RJ (1937) Relapsing febrile nodular nonsuppurative panniculitis (Weber-Christian disease). JAMA 109:1419–1425CrossRef
10.
Metadaten
Titel
Analysis of the clinical characteristics of thirteen patients with Weber-Christian panniculitis
verfasst von
Wei Zheng
Wenyuan Song
Qingqing Wu
Qiaoqiao Yin
Chaolan Pan
Hongying Pan
Publikationsdatum
12.08.2019
Verlag
Springer London
Erschienen in
Clinical Rheumatology / Ausgabe 12/2019
Print ISSN: 0770-3198
Elektronische ISSN: 1434-9949
DOI
https://doi.org/10.1007/s10067-019-04722-y

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