Results 71 to 80 of about 1,339 (137)

Common progenitor origin for Rosai–Dorfman disease and clear cell sarcoma

The Journal of Pathology, Volume 264, Issue 3, Page 243-249, November 2024.
Abstract Histiocytic neoplasms (HNs) in adults have been reported to be associated with a high prevalence of coexisting haematological and solid malignancies. While a proportion of coexisting HNs and haematological malignancies share identical genetic alterations, the genetic association between HNs and solid malignancies has scarcely been reported. We
Aki Sato, Nozomi Yusa, Hiroyuki Takamori, Eigo Shimizu, Kazuaki Yokoyama, Satoshi Ichikawa, Hisayuki Yokoyama, Yuki Kasahara, Kodai Enda, Fumiyoshi Fujishima, Ryo Ichinohasama, Yasunori Ota, Seiya Imoto, Yasuhito Nannya   +13 more
wiley   +1 more source

Persistent Generalized Lymphadenopathy: A Diagnostic Conundrum—Case Report and Review of Literature

Indian Journal of Medical and Paediatric Oncology
Generalized lymphadenopathy is a nonspecific sign with heterogenous etiology including infective, inflammatory, and malignant causes. We present the case of a child who presented with generalized lymphadenopathy, involving the cervical, axillary ...
Mahin Mundra, Vaishnavi Sreenivasan, Nisha Swami, Kawaldeep Kaur, Bhavika Rishi, Aroonima Misra, Sumit Mehndiratta, Amitabh Singh   +7 more
doaj   +1 more source

Severe acute liver disease in adults: Contemporary role of histopathology

Histopathology, Volume 85, Issue 4, Page 549-561, October 2024.
This overview provides an insight into the contemporary role of biopsies (as well as explant and autopsy material) in diagnosing acute liver disease. It outlines up‐to‐date clinical definitions of liver injury and considers recent recommendations for the diagnosis of AIH and drug‐induced, autoimmune‐like hepatitis (DI‐AIH).
Andrew D Clouston, Annette S H Gouw, Dina Tiniakos, Pierre Bedossa, Elizabeth M Brunt, Francesco Callea, Hans‐Peter Dienes, Zachary D Goodman, Stefan G Hubscher, Sanjay Kakar, David E Kleiner, Carolin Lackner, Young N Park, Eve A Roberts, Peter Schirmacher, Luigi Terracciano, Michael Torbenson, Ian R Wanless, Yoh Zen, Alastair D Burt   +19 more
wiley   +1 more source

Rosai-Dorfman disease of vertebra: Case report and literature review

The Turkish Journal of Pediatrics, 2016
Rosai-Dorfman disease is a rare benign histiocytic disorder that arises predominantly in lymph nodes with fever and malaise, but can affect various organs, with or without lymphadenopathy.
Zoran Igrutinovic, Rasa Medovic, Slavica Markovic, Gordana Kostic, Zorica Raskovic, Jelena Tanaskovic-Nestorovic, Marija Radovanovic, Biljana Vuletic   +7 more
doaj   +1 more source

Megakaryocyte emperipolesis in B‐lymphoblastic leukaemia

British Journal of Haematology, 2019
A 23-year-old male presented after a pre-syncopal episode and was found to have severe anaemia (haemoglobin concentration 50 g/l), neutropenia (neutrophils 0.5 9 10/l) and a normal platelet count (251 9 10/l).
M. Gurney, J. Krawczyk, Yizel E Paz Nuñez   +2 more
semanticscholar   +1 more source

Haga usted el diagnóstico: parte I

Revista de la Asociación Colombiana de Dermatología y Cirugía Dermatológica
Haga usted el diagnóstico: parte I. Se trata de un trastorno proliferativo histiocítico, raro y generalmente benigno que afecta principalmente los ganglios linfáticos cervicales, sin embargo, puede tener afectación de la piel en el 10% de los casos, se
Erika Muñoz-Herrera, Emil Jiménez-Berástegui, Juan David Ruiz-Restrepo   +2 more
doaj   +1 more source

Inhibition of CXCR1/2 reduces the emperipolesis between neutrophils and megakaryocytes in the Gata1low model of myelofibrosis

Experimental Hematology, 2023
Francesca Arciprete, Paola Verachi, F. Martelli, M. Valeri, M. Balliu, P. Guglielmelli, A. Vannucchi, A. Migliaccio, M. Zingariello   +8 more
semanticscholar   +1 more source

Soft Tissue Rosai-Dorfman Disease: Case report

Sultan Qaboos University Medical Journal, 2018
Rosai-Dorfman disease (RDD) is a rare benign proliferative histiocytic disorder characterised by massive lymphadenopathy. While extranodal involvement can occur in generalised RDD, isolated soft tissue RDD (STRDD) is extremely rare.
Rubyath C. Rajib, Rajasekharan Pillai, Ibrahim A. Sulaiman, Ibrahim Al-Haddabi   +3 more
doaj   +1 more source

Prominent emperipolesis in breast lesion: A diagnostic challenge

CytoJournal, 2023
Rishabh Sahai, Divya Singh, Vikas Shrivastava, Mukul Singh, Brijnandan Gupta   +4 more
semanticscholar   +1 more source

Clinical and Molecular Characteristics of Megakaryocytes in Myelodysplastic Syndrome

Global Medical Genetics
Objective Myelodysplastic syndrome (MDS) is a malignant clonal disorder of hematopoietic stem cells which is characterized by morphologic dysplasia.
Fangxiu Luo, Jialu Zhao, Yubao Chen, Zhenping Peng, Ran An, Yeling Lu, Jiaming Li   +6 more
doaj   +1 more source