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Journals / Turkish Journal of Hematology / 2009 / Cilt: 26 - Sayı: 2

Hiperfibrotik miyelodisplastik sendrom: Kuzey Hindistan’dan üç olgu sunumu

Hyperfibrotic myelodysplastic syndrome: A report of three cases from north India

Prasenjit DAS
Deepali JAIN
Reana DAS
Gurjeevan GAREWAL
Pages
93–96
DOI
—
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AI Summary & Key Takeaways

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

This entity should be classified separately in the chronic myeloproliferative disease (CMPD)-MDS group due to variable clinical presentation and poor prognosis.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Extensive fibrosis in myelodysplastic syndromes (MDS) is distinctly infrequent.
📊
Key Findings & Data:Herein, we report three rare cases of hyperfibrotic MDS.
💡
Conclusion & Impact:This entity should be classified separately in the chronic myeloproliferative disease (CMPD)-MDS group due to variable clinical presentation and poor prognosis.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Orta yaşlı · Lösemi · Primer miyelofibroz

Abstract

Extensive fibrosis in myelodysplastic syndromes (MDS) is distinctly infrequent. Herein, we report three rare cases of hyperfibrotic MDS. This entity should be classified separately in the chronic myeloproliferative disease (CMPD)-MDS group due to variable clinical presentation and poor prognosis.

Özet

Yaygın fibrozis miyelodisplastik sendromlarda (MDS) belirgin şekilde nadir görülmektedir. Biz burada üç nadir hiperfibrotik MDS olgusunu bildiriyoruz. Bu antite, değişken klinik tablo ve kötü prognozu nedeniyle kronik miyeloproliferatif hastalıklar (KMPH)-MDS grubu içinde ayrı olarak sınıflandırılmalıdır.

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Cite This Article

DAS, P., JAIN, D., DAS, R., GAREWAL, G. (2009). Hiperfibrotik miyelodisplastik sendrom: Kuzey Hindistan’dan üç olgu sunumu. Turkish Journal of Hematology, Cilt: 26 - Sayı: 2, 93–96. https://ajindex.com/articles/413381

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