Results 141 to 150 of about 24,352 (312)

Benign histiocyte-rich pseudotumor in post treatment mediastinal Hodgkin's lymphoma

Radiology Case Reports, 2020
Benign xanthomatous pseudotumors are rare, mass forming lesions composed of lipid laden histiocytes and tumor necrosis following chemotherapy.We present a rare case of young 36 year old male with primary mediastinal Hodgkin's lymphoma who developed ...
Yash Dilip Nilak, MBBS, DA, MRCP, Anjumara Nilak, MBBS, DMRE, DNB(Rad), MMED, FRCR, Salim Shafeek, MD FRCP FRCP(Ed) FRCPath(Haem), Dr. Zbigniew Rudzki, Joanne Chapman, BM, FRCPath, PGCE   +4 more
doaj  

Demystifying “Hyaline Angiopathy” of Pulse Granuloma in Oral and Extraoral Surgical Pathology

Oral Diseases, EarlyView.
ABSTRACT Background and Objectives Pulse granuloma (PG), or giant cell hyaline angiopathy, is an immune‐mediated reaction often following the implantation of plant‐derived food particles. PGs are primarily found in the oral cavity and gastrointestinal tract and may represent a histopathological pitfall, being mistaken for other granulomatous conditions
Felipe Fornias Sperandio, Matheus de Castro Costa, Marina Lara de Carli, Rani Kanthan   +3 more
wiley   +1 more source

Cavoatrial Bypass for Cardiac Complications From Rosai-Dorfman Disease

Annals of Thoracic Surgery Short Reports
Rosai-Dorfman disease (RDD) is a nonmalignant disease of histiocyte proliferation. RDD usually presents with painless cervical lymphadenopathy, although extranodal involvement can occur. Cardiac involvement was reported in
Quynh Nguyen, MD, Rachel Bourke, MD, Richard W. Gilbert, MD, Graziano Oldani, MD, Jong Moo Kim, MD, Andrew Lytle, MD, Richard C. Cook, MD, Hilary P. Grocott, MD, Joel Price, MD, MPH   +8 more
doaj  

Histopathological Patterns of Cutaneous and Mucocutaneous Leishmaniasis Due to L. aethiopica

Dermatology Research and Practice
Conclusion: In our study, the histopathological patterns of the CL caused by L. aethiopica were shown to have a dermal change that was characterized by a domination of diffused inflammatory cell infiltrate.
Abay Atnafu, Zewditu Chanyalew, Sofia Yimam, Meaza Zeleke, Shimelis Negussie, Selfu Girma, Aklilu Melaku, Menberework Chanyalew   +7 more
doaj   +1 more source

Macrophage-histiocytes in malignant lymphoma, small lymphocytic type (well-differentiated lymphocytic lymphoma) [PDF]

, 1985
H. J. Ree, James P. Crowley, Louis A. Leone   +2 more
openalex   +1 more source

Histiocytoid Sweet Syndrome With Paradoxical Neutropenia in a Pediatric Patient

Pediatric Dermatology, EarlyView.
ABSTRACT Histiocytoid Sweet syndrome (HSS) is a rare inflammatory skin condition characterized by the infiltration of mononuclear cells in the dermis and leukocytosis with neutrophilia. This uncommon variant of classic Sweet syndrome is rarely reported in the literature, especially in pediatric patients.
Shelby Boock, Stacey Blannett, Dominique Jacobs, Shane M. Swink   +3 more
wiley   +1 more source

T-zone histiocytes in adenocarcinoma of the lung in relation to postoperative prognosis [PDF]

, 1985
T Furukawa, Shaw Watanabe, Tetsuro Kodama, Yuichi Sato, Yukío Shimosato, Keiichi Suemasu   +5 more
openalex   +1 more source

Histiocytes in nasopharyngeal carcinoma in relation to prognosis [PDF]

, 1986
Hiroaki Nomori, Shaw Watanabe, Takashi Nakajima, Yukío Shimosato, Toru Kameya   +4 more
openalex   +1 more source

A rare case of lepromatous leprosy in Germany

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Roman Saternus, Gisela Bretzel, Tamaz Tsulaia, Kristin Burckhardt, Krista Yordanova, Sophie Elisabeth Müller, Steffen Jahn, Thomas Vogt, Sophie Schneitler   +8 more
wiley   +1 more source

Blau Syndrome (Juvenile Systemic Granulomatosis): State‐Of‐The‐Art Review

Pediatric Dermatology, EarlyView.
ABSTRACT Blau syndrome (BlauS) is a rare pediatric autoinflammatory disorder due to NOD2 gain‐of‐function pathogenic variants characterized by a triad of granulomatous dermatitis, arthritis, and uveitis, which can progress to systemic complications if untreated.
Ou Jia (Emilie) Wang, Marianna Jacob, Richard I. Crawford, Joseph M. Lam   +3 more
wiley   +1 more source