An unusual association between hemophagocytic lymphohistiocytosis, mixed connective tissue disease, and autoimmune hemolytic anemia: A case report

RATIONALE: In the adult patient, hemophagocytic lymphohistiocytosis (HLH) is uncommon and frequently difficult to diagnose due to its nonspecific presentation and numerous complications. PATIENT CONCERNS: Herein, we present the case of a 25-year-old female who initially presented for evaluation of p...

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Detaylı Bibliyografya
Yayımlandı:Medicine (Baltimore)
Asıl Yazarlar: Kelkar, Amar H., Shah, Anushi A., Yong, Sherri L., Ahmed, Zohair
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Wolters Kluwer Health 2017
Konular:
4800
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5515764/
https://ncbi.nlm.nih.gov/pubmed/28700492
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000007488
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