Malignant histiocytosis

1980 ◽  
Vol 58 (1) ◽  
pp. 31-35 ◽  
Author(s):  
D. Huhn ◽  
P. Meister ◽  
W. Wilmanns
Keyword(s):  
Malignant Histiocytosis

Clonal evolution in cutaneous malignant histiocytosis

1985 ◽  
Vol 10 (2) ◽  
pp. 121-126 ◽  
Author(s):  
GUNHILD LANGE WANTZIN ◽  
ELISABETH RALFKIAER ◽  
JORGEN K. LARSEN ◽  
KRISTIAN THOMSEN
Keyword(s):  
Clonal Evolution ◽  
Malignant Histiocytosis

HEAD AND NECK INVOLVEMENT WITH MALIGNANT HISTIOCYTOSIS

1981 ◽  
Vol 91 (6) ◽  
pp. 982???987 ◽  
Author(s):  
SUSAN L. LUEDKE ◽  
DAN W. LUEDKE ◽  
KEVIN MCCABE
Keyword(s):  
Head And Neck ◽  
Malignant Histiocytosis

Fulminant Multisystem Non–Langerhans Cell Histiocytic Proliferation With Hemophagocytosis

2005 ◽  
Vol 129 (2) ◽  
pp. e39-e43 ◽  
Author(s):  
R. Nagarjun Rao ◽  
Chung-che Chang ◽  
Nevin Uysal ◽  
Kenneth Presberg ◽  
Vinod B. Shidham ◽  
...  
Keyword(s):  
Langerhans Cell Histiocytosis ◽  
Clinical Course ◽  
Langerhans Cell ◽  
Variant Form ◽  
Malignant Histiocytosis ◽  
Unique Case ◽  
Multiple Organs ◽  
Biopsy Specimens ◽  
Extensive Involvement ◽  
Erdheim Chester

Abstract Hemophagocytosis (HP), a feature seen in malignant histiocytosis and infection- and lymphoma-associated disorders, has not been previously emphasized in Erdheim-Chester disease (ECD). Generally, ECD is recognized as a rare, systemic, non–Langerhans cell histiocytosis with a variable clinical course. Herein, we describe a unique case of multisystem non–Langerhans cell histiocytic proliferation with a fulminant clinical course (death occurred within 3 months of presentation) that showed prominent HP and extensive involvement of multiple organs, including the lungs, resulting in respiratory failure. Hemophagocytosis led to severe anemia that required transfusion and thrombocytopenia. Antemortem lung and bone marrow biopsy specimens revealed involvement by a histiocytic infiltrate with features highly suggestive of ECD and HP. Furthermore, the autopsy documented the presence of HP and the histiocytic infiltrate in multiple other organs. This case is best categorized as a variant form of ECD. Recognizing this variant has the following important implications: (1) HP may be a marker for fulminant clinical course in ECD, (2) the presence of HP does not exclude a diagnosis of ECD, and (3) ECD should be considered in the differential diagnosis of HP.

Erythema annulare centrifugum and malignant histiocytosis-report of a case

1984 ◽  
Vol 9 (6) ◽  
pp. 608-613 ◽  
Author(s):  
H.J. DODD ◽  
J.D.T. KIRBY ◽  
T.J. CHAMBERS ◽  
A.G. STANSFELD
Keyword(s):  
Malignant Histiocytosis ◽  
Erythema Annulare Centrifugum

scholarly journals KRAS mutation in secondary malignant histiocytosis arising from low grade follicular lymphoma

2018 ◽  
Vol 13 (1) ◽  
Author(s):  
Sarah M. Choi ◽  
Aleodor A. Andea ◽  
Min Wang ◽  
Amir Behdad ◽  
Lina Shao ◽  
...  
Keyword(s):  
Follicular Lymphoma ◽  
Kras Mutation ◽  
Low Grade ◽  
Malignant Histiocytosis

scholarly journals A Case of Canine Malignant Histiocytosis

1998 ◽  
Vol 51 (5) ◽  
pp. 259-262
Author(s):  
Takuji TSUDA ◽  
Shinji SHIBATA ◽  
Takeshi SHIBATA ◽  
Kosaku FUJIWARA
Keyword(s):  
Malignant Histiocytosis
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