Journals / Ahi Evran Tıp Dergisi / 2026 / Volume: 8 Issue: 2

A Case of Sarcoidosis with Atypical Presentation

Atipik Prezentasyon Gösteren Sarkoidoz Olgusu

Duygu Acer(Ankara Şehir Hastanesi)0009-0006-5988-085X
Mehmet Veysel Coşkun(Sivrihisar Devlet Hastanesi)0000-0002-6626-9518
Ali Can Kurtipek(ANKARA UNIVERSITY, ANKARA FACULTY OF MEDICINE)0000-0002-3504-7402
Pages
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Publication Date
2024-08-27
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AI Summary & Key Takeaways

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

Here, we aim to present a case of extrapulmonary sarcoidosis diagnosed after excluding Macrophage Activation Syndrome and lymphoma during clinical follow-up.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Sarcoidosis is a multisystemic disease characterized by non-caseating granulomas of unknown etiology.
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Key Findings & Data:While pulmonary manifestations are present in 90% of cases, extrapulmonary sarcoidosis cases are rare and diagnosis is often challenging due to atypical clinical course.
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Conclusion & Impact:Here, we aim to present a case of extrapulmonary sarcoidosis diagnosed after excluding Macrophage Activation Syndrome and lymphoma during clinical follow-up.
🔬Design:Case Report
📍Scope:Comprehensive Sample
⚙️Variables:lymphoma · macrophage activation syndrome · sarcoidosis

Abstract

Sarcoidosis is a multisystemic disease characterized by non-caseating granulomas of unknown etiology. While pulmonary manifestations are present in 90% of cases, extrapulmonary sarcoidosis cases are rare and diagnosis is often challenging due to atypical clinical course. Here, we aim to present a case of extrapulmonary sarcoidosis diagnosed after excluding Macrophage Activation Syndrome and lymphoma during clinical follow-up.

Özet

Sarkoidoz, nonkazeifiye granülomlarla karakterize, etiyolojisi bilinmeyen multisistemik bir hastalıktır. Olguların %90'ında akciğer bulguları mevcut olmakla birlikte, ekstrapulmoner sarkoidoz olguları oldukça nadirdir ve atipik klinik seyir nedeniyle tanı koymak genellikle zordur. Burada klinik takibinde Makrofaj aktivasyonu sendromu ve lenfoma ekarte edildikten sonra tanısı konulan bir ekstrapulmoner sarkoidoz olgusunu sunmayı amaçladık.

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Cite This Article

Acer, D., Coşkun, M. V., Karaahmetoğlu, S., Kurtipek, A. C. (2024). A Case of Sarcoidosis with Atypical Presentation. Ahi Evran Tıp Dergisi, Volume: 8 Issue: 2. https://doi.org/10.46332/aemj.1381010

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References (9)

  1. Judson MA. The Clinical Features of Sarcoidosis: A Comprehensive Review. Clin Rev Allergy Immunol. 2015;49(1):63-78.
  2. Sharma OP. Sarcoidosis: clinical, laboratory, and immunologic aspects. Semin Roentgenol. 1985;20(4): 340-355.
  3. Rao DA, Dellaripa PF. Extrapulmonary manifestations of sarcoidosis. Rheum Dis Clin North Am. 2013;39(2):277-297.
  4. Marchell RM, Judson MA. Cutaneous sarcoidosis. Semin Respir Crit Care Med. 2010;31(4):442-451.
  5. Wanat KA, Rosenbach M. Cutaneous Sarcoidosis. Clin Chest Med. 2015;36(4):685-702.
  6. Selroos O. Sarcoidosis of the spleen. Acta Med Scand. 1976;200(1-6):337-340.
  7. Kataria YP, Whitcomb ME. Splenomegaly in sarcoidosis. Arch Intern Med. 1980;140(1):35-37.
  8. Sharma OP, Vucinic V, James DG. Splenectomy in sarcoidosis: indications, complications, and long-term follow-up. Sarcoidosis Vasc Diffuse Lung Dis. 2002;19(1):66-70.
  9. Modi T, Maniam G, Quirch M, et al. Extrapulmonary sarcoidosis in an atypical patient demographic. Proc (Bayl Univ Med Cent). 2020;34(1):151-152.