Literature DB >> 24628074

Cutaneous Langerhans cell histiocytosis in elderly with chronic myelomonocytic leukemia.

Takeshi Iwasaki1, Ichiro Takahashi, Takahiro Nagashima, Satomi Igawa, Shigetsuna Komatsu, Masaru Honma, Akemi Ishida-Yamamoto, Hajime Iizuka.   

Abstract

Langerhans cell histiocytosis (LCH) is a rare histiocytic neoplasm characterized by clonal proliferation of Langerhans cells in multi-organ systems including skin, bone, pituitary gland, liver and spleen. Skin-limited involvement of LCH usually indicates an indolent clinical course; however, in rare cases, LCH is accompanied by other myeloproliferative disorders, which may determine the prognosis. An 82-year old Japanese man presented with numerous asymptomatic facial papules clinically simulating rhinophyma. Although findings of histopathology and general examination including bone marrow biopsy led to the diagnosis of cutaneous LCH, he died from chronic myelomonocytic leukemia, which emerged 10 months after the initial diagnosis of LCH. The previously reported cases of LCH concomitant with other hematological disorders are also summarized and described compared with the present case.
© 2014 Japanese Dermatological Association.

Entities:  

Keywords:  Langerhans cell histiocytosis; myelodysplastic syndrome; myelomonocytic leukemia; rhinophyma; systemic steroid

Mesh:

Year:  2014        PMID: 24628074     DOI: 10.1111/1346-8138.12417

Source DB:  PubMed          Journal:  J Dermatol        ISSN: 0385-2407            Impact factor:   4.005


  1 in total

1.  Coexisting BRAF-Mutated Langerhans Cell Histiocytosis and Primary Myelofibrosis with Shared JAK2 Mutation.

Authors:  Johanne Marie Holst; Marie Beck Enemark; Trine Lindhardt Plesner; Martin Bjerregaard Pedersen; Maja Ludvigsen; Francesco d'Amore
Journal:  Case Rep Hematol       Date:  2021-04-16
  1 in total

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