Results 101 to 110 of about 13,665 (250)

Multiple primary malignancy: a report on Langerhans cell histiocytosis associated with Hodgkin's disease

The Turkish Journal of Pediatrics, 1991
Since multiple primary malignant tumors are rare in children, their presence can be a diagnostic and therapeutic problem. In this report, we present a six-year-old boy with Langerhans cell histiocytosis and Hodgkin's disease.
C Karadeniz, F Sarialioğlu, S Göğüş, C Akyüz, T Küçükali, T Kutluk, M Büyükpamukçu   +6 more
doaj  

Occurrence of mesothelial/monocytic incidental cardiac excrescences in material from open-heart procedures: case reports and literature review

Autopsy and Case Reports, 2018
Mesothelial/monocytic incidental cardiac excrescences (MICE) are unusual findings during the histological analysis of material from the pericardium, mediastinum, or other tissues collected in open-heart surgery.
Vitor Gabriel Ribeiro Grossi, Karen Lee, Léa Maria Demarchi, Jussara Bianchi Castelli, Vera Demarchi Aiello   +4 more
doaj   +1 more source

High viral load of Merkel cell polyomavirus DNA sequences in Langerhans cell sarcoma tissues. [PDF]

, 2014
International audienceBACKGROUND: Langerhans cell (LC) sarcoma (LCS) is a high-grade neoplasm with overtly malignant cytologic features and an LC phenotype.
A Kanik, A Kubo, C Pancaldi, CET da Costa, D Schrama, D Tortorella, DP O'Malley, E Izmailova, Francis Jaubert, H Feng, Hirokazu Nakamine, I Grosjean, I Murakami, Ichiro Murakami, J Banchereau, J Engelmayer, Jean Gogusev, Katsuyoshi Takata, Kazuhiko Hayashi, KD Mertz, KJ Busam, M Matsushita, M Shamoto, M Shuda, Masako Kato, Michiko Matsushita, Mitsunori Yamakawa, R Jaffe, S Kuwamoto, S Kuwamoto, S Weitzman, Satoshi Kuwamoto, Shu Nakamoto, Tadashi Yoshino, Takashi Oka, Takeshi Iwasaki, X Sastre-Garau, Yasushi Horie, YL Tolstov   +38 more
core   +4 more sources

Angiotensin converting enzyme and malignant histiocytosis [PDF]

, 1983
J R Hobbs
openalex   +1 more source

New cases expand the genotype, phenotype and therapeutic landscape of H syndrome

British Journal of Haematology, Volume 208, Issue 1, Page 363-366, January 2026.
Clément Triaille, Julie Beauchemin, Philippe M. Campeau, Hugo Chapdelaine, Julie Dery, Maria Kondyli, Grant Mitchell, Julie Powell, Sophie Turpin, Guilhem Cros, Fabien Touzot   +10 more
wiley   +1 more source

Asymptomatic flow of Rosai-Dorfman disease [PDF]

, 2014
Introduction. Sinus histiocytosis with massive lymphadenopathy is a rare benign self-limiting disease of unknown etiology. The salivary gland involvement, indicating the extranodal character of the disease, often presents a diagnostic dilemma ...
Bjelaković Bojko, Kesić Ljiljana, Kostić Miloš, Mihailović Dragan, Mijovićć Žaklina, Petrović Dragan, Petrović Milica, Petrović Slađana, Stanković Ana, Vučković Ivica, Živković Nikola   +10 more
core   +1 more source

A novel translocation, t(2;5)(p23;q35), in childhood phagocytic large T- cell lymphoma mimicking malignant histiocytosis [PDF]

, 1989
Yasuhiko Kaneko, Glauco Frizzera, S Edamura, Nobuo Maseki, M Sakurai, Yoshihiro Komada, M Sakurai, H Tanaka, M. Sasaki, Taizan Suchi   +9 more
openalex   +3 more sources

Concomitant sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease) and diffuse large B-cell lymphoma: a case report

Journal of Medical Case Reports, 2008
Introduction Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman Disease, is a rare and benign source of lymphadenopathy first described in 1969, which mimics neoplastic processes.
Moore James C, Zhao Xiaohui, Nelson Edward L   +2 more
doaj   +1 more source

EPSTEIN-BARR-VIRUS ASSOCIATED SYNDROMES IN IMMUNOSUPPRESSED LIVER-TRANSPLANT RECIPIENTS - CLINICAL PROFILE AND RECOGNITION ON ROUTINE ALLOGRAFT BIOPSY [PDF]

, 1990
The clinical profile and histopathologic changes in needle biopsies of the liver were studied in 10 cases of acute Epstein-Barr virus infection occurring in liver transplant recipients.
DEMETRIS, AJ, MARKIN, RS, RANDHAWA, PS, STARZL, TE   +3 more
core   +1 more source

Exploration of treatment in childhood Langerhans cell histiocytosis based on inflammatory and malignant symptoms: a pilot study

Orphanet Journal of Rare Diseases
Background Multisystem childhood Langerhans cell histiocytosis (LCH) patients, especially those with risk organ (RO) involved, had not been satisfactorily treated under the international traditional schemes as high incidences of reactivation with late ...
Hui-ling Lin, Qing-qing Zheng, Ru-lin Huang, Rong Hu, Xiao-dan Liu, Jia-yi Wang   +5 more
doaj   +1 more source