Results 111 to 120 of about 13,665 (250)

Rosai - Dorfman disease: a rare entity diagnosed at autopsy

Autopsy and Case Reports, 2013
Rosai-Dorfman disease (RDD) or Sinus histiocytosis with massive lymphadenopathy is a rare and benign histiocytic proliferative disorder first described by Juan Rosai and Ronald Dorfman in 1969, whose etiology remains unknown.
João da Costa Veloso Neto, Sheila Aparecida Coelho Siqueira, Maria Claudia Nogueira Zerbini   +2 more
doaj   +1 more source

Bronchiolitis obliterans. [PDF]

, 1989
Bronchiolitis obliterans in the adult patient is a relatively uncommon and vexing clinical entity. This confusion results because this pathologic finding occurs in a variety of diverse clinical settings.
King, TE
core  

Malignant histiocytosis. Report of five chinese patients [PDF]

, 1978
Faith Ho, D. Todd
openalex   +1 more source

Bone marrow transplantation for malignant histiocytosis in childhood [PDF]

, 1985
Marcus R. Vowels, R Lam-Po-Tang, Hedy Mameghan, EDGAR H. HELLER, David Ford, John B. Ziegler, Darcy O'Gorman Hughes   +6 more
openalex   +1 more source

Malignant histiocytosis. Response to VP-16-213 and cytosine arabinoside [PDF]

, 1984
Raúl Vera, Joseph R. Bertino, E Cadman, James A. Waldron   +3 more
openalex   +1 more source

Mucosa associated lymphoid tissue lymphoma of the thyroid gland: a case report and literature review = MALT linfoma della tiroide: caso clinico e revisione della letteratura [PDF]

, 2012
Mucosa associated lymphoid tissue (MALT) lymphomas are low-grade, non-Hodgkin’s B cell lymphomas, mainly occurring in the gastrointestinal tract, but also in other tissues.
Attene, Federico, Paliogiannis, Panagiotis, Pisano, Ilia Patrizio, Pulighe, Fabio, Scognamillo, Fabrizio, Trignano, Mario   +5 more
core  

Growing intradiploic epidermoid cyst presenting as a diagnostic challenge in the setting of Langerhans cell histiocytosis: A case report

Radiology Case Reports
Epidermoid cysts (EC) are benign cystic lesions lined by squamous epithelium resulting from entrapped ectodermal elements during development. These can occur in various anatomic locations, including intracranial, intradiploic, spinal and in the ...
Benjamin S. Fletcher, MD, Benjamin A. Johnson-Tesch, MD, John C. Benson, MD, Alex A. Nagelschneider, MD, Lisa M. Marinelli, MD, Dong Kun Kim, MD   +5 more
doaj   +1 more source

Multicentric reticulohistiocytosis revealing a ductal breast cancer in situ: A case report with dermoscopic and histopathological findings

Medwave
Multicentric reticulohistiocytosis is a rare non-Langerhans cell histiocytosis of unknown etiology. It is classified as multicentric because of multisystem involvement.
Sofía Palma Peña, Gabriel Neely Erdos, Catalina Buchroithner Haase, Claudio Pinto Viguera   +3 more
doaj   +1 more source

A neonatal pustule:Langerhans cell histiocytosis [PDF]

, 2019
Langerhans cell histiocytosis (LCH) is a rare, clinically heterogeneous disease that most commonly occurs in pediatric populations. Congenital self-limited LCH is a benign variant of LCH.
Hogeling, Marcia, Kang, Yuna, Knowles, Byron, McKenzie, Shanice, Vecerek, Natalia   +4 more
core  

Disseminated Malignant Histiocytosis in a Golden Retriever: Clinicopathologic, Ultrastructural, and Immunohistochemical Findings [PDF]

, 1993
David W. Hayden, David J. Waters, Barbara A. Burke, J. Carlos Manivel   +3 more
openalex   +1 more source