Bone Marrow Langerhans Cell Histiocytosis in Association with Kasabach-Merritt Syndrome: The Difficulty of a Differential Diagnosis

Langerhans cell histiocytosis is a rare haematological disorder with variable clinical findings and a high mortality rate. On the other hand, Kasabach-Merritt syndrome is of rare onset at adult age, requiring the simultaneous presentation of vascular lesion, thrombocytopenia, and consumptive coagulo...

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Detalles Bibliográficos
Autores principales: Serra, Joao Tiago, Silva, Raquel, Aldomiro, Fernando, Duarte, Fernanda Paixao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184841/
https://www.ncbi.nlm.nih.gov/pubmed/32355498
http://dx.doi.org/10.1159/000506539

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184841/
https://www.ncbi.nlm.nih.gov/pubmed/32355498
http://dx.doi.org/10.1159/000506539

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