Journals / Türk Göğüs Kalp Damar Cerrahisi Dergisi / 2009 / Cilt: 17 - Sayı: 3

Castleman hastalığı: Nadir iki olgu sunumu

Castleman’s disease: A report of two rare cases

Pages
210–213
Publication Date
2022-09-02
DOI
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AI Summary & Key Takeaways

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

We report two unusual thoracic manifestations of Castleman’s disease with chest wall and intraparenchymal location, the latter of which is extremely rare.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Castleman’s disease is a rare lymphoproliferative disorder, which usually occurs in the chest.
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Key Findings & Data:A 43-year-old woman who had a history of dry cough for the last six months and a 24-year-old man who had a right anterior chest pain complaint for a year were admitted to our clinic.
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Conclusion & Impact:We report two unusual thoracic manifestations of Castleman’s disease with chest wall and intraparenchymal location, the latter of which is extremely rare.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Castleman’s disease is a rare lymphoproliferative disorder, which usually occurs in the chest. The localized form, which is the most common, is often asymptomatic, but can cause nonspecific thoracic symptoms such as cough and dyspnea. Surgical removal is the choice of approach for the management of such cases, in both confirming the diagnosis and curative treatment. A 43-year-old woman who had a history of dry cough for the last six months and a 24-year-old man who had a right anterior chest pain complaint for a year were admitted to our clinic. Thorax computed tomography of cases showed a right hilar well-defined intraparenchymal lesion in the former one and a mass lesion located on the right anterior chest wall in the latter. Surgical intervention was planned in both cases. Histopathological examination of the surgical specimen of both cases revealed hyaline vascular type Castleman’s disease. We report two unusual thoracic manifestations of Castleman’s disease with chest wall and intraparenchymal location, the latter of which is extremely rare.

Özet

Castleman hastalığı, genellikle göğüs boşluğunda görülen, lenf nodu proliferasyonu ile seyreden nadir bir hastalıktır. Yerleşik formu çok daha sık görülür ve sıklıkla semptom vermez, fakat dispne ve öksürük gibi nonspesifik torasik semptomlara neden olabilir. Hem kesin tanı hem de küratif tedavi için cerrahi, seçilecek iyi bir yaklaşımdır. Son altı aydır kuru öksürüğü olan 43 yaşında bayan hastanın ve son bir yıldır sağ göğüs ağrısı olan 24 yaşında erkek hastanın çekilen göğüs tomografilerinde; ilk olguda sağ hilusda parenkim içinde, ikinci olguda ise sağ göğüs ön duvarında düzgün sınırlı, kitle lezyon tespit edildi. Her iki olguda da cerrahi planlandı ve ameliyat sonrası histopatolojik değerlendirmede her ikisi de, hiyalin vasküler tip Castleman hastalığı olarak raporlandı. Bu makalede, Castleman hastalığının çok nadir görülen, parenkim içi ve göğüs duvarı olmak üzere iki intratorasik yerleşimi sunuldu. Bunlardan parenkim yerleşimli olan tipi son derece nadir görülür.

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Cite This Article

VURAL, S., AKGÜN, M., YEKELER, E., ERDOĞAN, F. (2022). Castleman hastalığı: Nadir iki olgu sunumu. Türk Göğüs Kalp Damar Cerrahisi Dergisi, Cilt: 17 - Sayı: 3, 210–213. https://ajindex.com/articles/425008

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