Results 61 to 70 of about 18,484 (199)

HISTIOCITOSE DE CÉLULAS NÃO LANGERHANS PEDIÁTRICA - UM CASO ATÍPICO [PDF]

, 2015
Introduction: Histiocytoses correspond to a heterogeneous group of disorders characterized by the proliferation and infiltration of histiocytes in tissues.
Alves, Rosário, Coelho, Sandrina, Machado, Susana, Selores, Manuela, Vasconcelos, Gabriela   +4 more
core   +2 more sources

Histomorphological analysis and clinical correlation of neoplastic and non neoplastic skin lesions: a study in a tertiary care centre of Western Uttar Pradesh, India [PDF]

, 2020
Background: Clinical examination may suffice in making diagnosis of most dermatologic disorders but histopathological examination is often required to confirm the diagnosis and further categorize the lesions. Authors carried out this study to analyse the
Arya, Anjana, Bisht, Mithila, Choudhry, B. C.   +2 more
core   +2 more sources

Diffuse plane xanthomas as the first manifestation of multiple myeloma

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Eleni Koutra, Elke Lusmöller, Hosam Ghanem, Astrid Aumann, Jens Atzpodien, Rudolf Stadler   +5 more
wiley   +1 more source

Frequency and Implications of High‐Risk Pharmacogenomic Phenotypes Identified in a Diverse Australian Pediatric Oncology Cohort

Clinical and Translational Science, Volume 18, Issue 5, May 2025.
ABSTRACT Pharmacogenomics remains underutilized in pediatric oncology, despite the existence of evidence‐based guidelines. Implementation of pharmacogenomics‐informed prescribing could improve medication safety and efficacy in pediatric oncology patients, who are at high risk of adverse drug reactions.
Claire Moore, Andreas Halman, Tayla Stenta, Dhrita Khatri, Elizabeth Williams, Roxanne Dyas, Julian Stolper, David A. Elliott, Rachel Conyers   +8 more
wiley   +1 more source

A Case of Indeterminate Cell Histiocytosis in an Infant [PDF]

, 2007
Indeterminate cell histiocytosis is a rare disease of predominant cells having features that resemble both Langerhans cells and macrophages. The cells have greater pleomorphism with polyobated nuclei and these cells express markers for macrophages and ...
유철주
core  

Application of Human Papillomavirus‐DNA Test on Salivary Gland Fine Needle Aspiration Cytology Samples Confirms the Absence of the Virus in Primary Neoplasms and Demonstrates for the First Time Its Presence in Salivary Intraglandular Cysts

Diagnostic Cytopathology, Volume 53, Issue 3, Page 127-135, March 2025.
ABSTRACT Background The correlation between Human Papillomavirus (HPV) and salivary gland neoplasms is still controversial. Data in the literature are conflicting, reporting the presence of the HPV‐DNA in a significant percentage of cases or none. We investigated the presence of HPV in a series of salivary gland neoplasms using fine needle aspiration ...
Immacolata Cozzolino, Andrea Ronchi, Marco Montella, Raffaella Ruggiero, Rosaria Cappiello, Giovanni Savarese, Giuseppe Colella, Renato Franco   +7 more
wiley   +1 more source

A Rare Case Report: A Malignant Histiocytic Tumor in the Form of Ovarian Mass [PDF]

, 2018
Histiocytic cell malignancies are very rare. Hence, the information about this disease in hematology is limited. In this case report, we present a case of malignant histiocytic tumor affecting the ovary of a 40-year-old virgin female.
Emsal Pinar Topdagi Yilmaz, Seray Kaya Topdagi, Yakup Kumtepe, Yunus Emre Topdagi   +3 more
core   +2 more sources

Features of gastrointestinal acute graft‐versus‐host disease in children undergoing hematopoietic stem cell transplantation

Journal of Pediatric Gastroenterology and Nutrition, Volume 80, Issue 2, Page 271-281, February 2025.
Abstract Objectives Graft‐versus‐host disease (GVHD) commonly affects the gastrointestinal (GI) tract among children who undergo hematopoietic stem cell transplantation (HSCT). Studies concerning GI‐acute GVHD (aGVHD) in developing countries are limited.
Kritiya Rattanaseksan, Usanarat Anurathapan, Pornthep Tanpowpong   +2 more
wiley   +1 more source

Neurology and the histiocytoses: a case of Rosai-Dorfman-Destombes disease [PDF]

, 2022
The histiocytoses are a group of rare disorders characterised by the accumulation of neoplastic or non-neoplastic activated histiocytes in various tissues.
Blake, Julian, Bremner, Fion D, Carroll, Antonia S, D'Sa, Shirley, Doherty, Carolynne M, Hoskote, Chandrashekar, Hunt, Stephen J, McNamara, Christopher, McNicholl, Feargal, Phadke, Rahul, Reilly, Mary M, Sheehy, Oonagh   +11 more
core  

Cutaneous Rosai–Dorfman disease with MAP2K1 mutation, initially mimicking an infection with parasitized histiocytes

Journal of Cutaneous Pathology, Volume 51, Issue 12, Page 942-947, December 2024.
Abstract Rarely, Rosai–Dorfman disease (RDD) manifests exclusively in the skin, typically as nodules on the trunk and extremities. Recognition of characteristic histopathologic features enables diagnosis of RDD. A 55‐year‐old female presented with a 7‐year history of cutaneous nodules involving the trunk and extremities. A prior skin biopsy specimen at
Joseph Gillam, Ruchi Desai, Raphael J. Louie, Scott A. Turner, Grace Y. Wang, Julio A. Diaz‐Perez, Mark C. Mochel   +6 more
wiley   +1 more source