Results 131 to 140 of about 55,121 (305)

Histiocytosis X with involvement of brain [PDF]

, 1967
Joseph Rubé, Samuel de la Pava, John W. Pickren   +2 more
openalex   +1 more source

Intestinal Langerhans cell histiocytosis presenting with symptoms similar to inflammatory bowel disease: a case report

Pathology and Oncology Research
Background:Langerhans cell histiocytosis is a rare disease characterized by the abnormal proliferation of Langerhans cells within a single organ or multiple organs.
Yuqing Liu, Zhenwei Chen, Lu Wang, Baizhou Li   +3 more
doaj   +1 more source

Clinical, histochemical, and electron microscopic study of colonic histiocytosis. [PDF]

, 1966
Fred E. Pittman, William Smith, Aya Mizrahi, William A. Blanc, Joan C. Pittman   +4 more
openalex   +1 more source

Splenic sea-blue (ceroid) histiocytosis due to hypertriglyceridemia: Report of a case and review of literature

Human Pathology: Case Reports, 2017
Sea-blue histiocytosis is a rare condition that can be often identified in bone marrow, spleen, liver as well as other organs. It can be frequently detected in bone marrow of patients with myeloproliferative neoplasms as well as non-neoplastic conditions
Kacy A. Krehbiel, Robert H. Glew, Sheila Modi, Mohammad A. Vasef   +3 more
doaj  

Rheumatological manifestations of H syndrome

Rheumatology
H syndrome (HS) is a rare autosomal recessive genodermatosis characterised by cutaneous hyper­pigmentation, hypertrichosis, sclerodermatous thickening, and multisystemic involvement.
Honsali Rahma, Latifa Tahiri, Sara Cherkaoui Dekkaki, Fadoua Allali   +3 more
doaj   +1 more source

A pure Cutaneous Rosai-Dorfman disease: case report and a review of the literature

Caspian Journal of Internal Medicine, 2022
Background: Cutaneous Rosai-Dorfman disease (CRDD) is a rare variant of benign histiocytic proliferative disorder limited to the skin. The underlying etiology is still unclear, but it had been claimed that infections, immunodeficiencies, and autoimmune ...
Fatemeh Montazer, Saeedeh Farahani, Zoha Shaka, Zeinab Aryanian, Azadeh Goodarzi   +4 more
doaj  

Rod-like tubular structures in the cytoplasm of histiocytes in “histiocytosis X” [PDF]

, 1968
Jie Man
openalex   +1 more source

Case report: Uncommon manifestations of Rosai-Dorfman disease in the liver mimicking HCC

Frontiers in Oncology
Rosai-Dorfman-Destombes disease (RDD) is a rare non-Langerhans cell histiocytosis (LCH) disorder characterized by systemic extranodal lesions. Common cases include skin lesions, whereas liver lesions are rare.
Huipeng Ren, Hao Zhang, Qinyun Wan, Yuhui Pang, Hongzhe Tian, Zhuanqin Ren, Yuan Cai   +6 more
doaj   +1 more source

Sinus histiocytosis with massive lymphadenopathy: A pseudolymphomatous benign disorder.Analysis of 34 cases [PDF]

, 1972
Juan Rosaí, Ronald F. Dorfman
openalex   +1 more source

Malignant histiocytosis (histiocytic medullary reticulosis).I. Clinicopathologic study of 29 cases [PDF]

, 1975
Roger A. Warnke, Hun Kim, Ronald F. Dorfman   +2 more
openalex   +1 more source