Results 81 to 90 of about 6,359 (165)

Erdheim–Chester Disease Manifesting Without Long Bone Involvement

Respirology Case Reports
Erdheim–Chester Disease (ECD) is an extremely rare, non‐Langerhans cell histiocytosis characterised by the proliferation of foamy histiocytes infiltrating various organs.
Dhiran Sivasubramanian, Karthick Balasubramanian, Mohamed Raghib Hussain Mohamed Kalifa, Sathwik Sanil, Smrti Aravind, Nithish Nanda Palanisamy, Virushnee Senthilkumar   +6 more
doaj   +1 more source

Erdheim–Chester disease: A multisystem non-Langerhans cell histiocytosis with cutaneous involvement

Journal of the Royal College of Physicians of Edinburgh
Erdheim–Chester disease (ECD) is a rare non-Langerhans cell histiocytosis (LCH) marked by systemic involvement and diverse clinical manifestations. We report a 35-year-old man with yellowish-brown periorbital lesions initially diagnosed as xanthelasma, which later recurred.
Neetu Bhari, Ritu Sharma, Sushant Agrawal, Vishal Gaurav   +3 more
openaire   +1 more source

Case report: Pulmonary non-Langerhans cell histiocytosis in a dog with acute interstitial granulomatous pneumonia

Frontiers in Veterinary Science
BackgroundPulmonary involvement of Non-Langerhans Cell Histiocytosis (PNLCH) is a rare cause of interstitial pulmonary disease in people and are classified as either Erdheim-Chester disease (ECD) or Rosai-Dorfman disease (RDD). In veterinary medicine, feline pulmonary Langerhans cell histiocytosis (PLCH) has been identified as an infiltrative ...
Kyle L. Granger, Kurt Williams, Alex Ohlendorf, Sarah Shropshire, Kelly E. Hall   +4 more
openaire   +3 more sources

Generalized indeterminate cell histiocytosis successfully treated with methotrexate

JAAD Case Reports, 2022
Erina Lie, MD, Jaroslaw Jedrych, MD, Ronald Sweren, MD, Michelle L. Kerns, MD   +3 more
doaj   +1 more source

Non-langerhans cell histiocytosis involving the spleen - Erdheim-Chester disease: a case report

REVISTA DELOS
Erdheim-Chester Disease (ECD) is a rare form of non-Langerhans histiocytosis characterized by the proliferation of CD68+, CD1a-, and CD163+ histiocytes, with potential multisystem involvement. We report the case of a 31-year-old male presenting with refractory abdominal pain and splenomegaly.
Giovanna Lage Fagunde, Luiza Guimarães Vidigal, Otávio Gabriel Lopes, Alexandre Venâncio de Sousa   +3 more
openaire   +1 more source

NON-LANGERHANS CELLS HISTIOCYTOSIS ASSOCIATED WITH SYSTEMIC LUPUS ERYTHEMATOSUS - CASE REPORT

SBR 2021 Congresso Brasileiro de Reumatologia, 2021
Izaura Tereza Silva Guedes, Edgard Torres dos Reis Neto, Renan Rodrigues Neves Ribeiro do Nascimento, Isaac Felipe Leite Braz, Miriam Fang Castro, Rodrigo Lorenzetti Serrano, Guilherme Pereira Carlesso, Felipe de Lacerda Veiga, Lucas de Castro Barroti, Leonardo Afonso Costa, João Paulo Peres Lima   +10 more
openaire   +1 more source

Langerhans cell histiocytosis manifesting at birth: a neonatal case with BRAF V600E mutation. [PDF]

Diagn Pathol
Tang W, Wang P.
europepmc   +1 more source

Multisystem Langerhans cell Histiocytosis presenting with spontaneous pneumothorax in a toddler: case report and literature review. [PDF]

Oxf Med Case Reports
Tard SC, Shrivastav A, Tanwar GS, Beniwal M.   +3 more
europepmc   +1 more source

Introduction to the Review Series. Looking back and to the future: the Histiocyte Society blueprint for research in histiocytic disorders. [PDF]

Haematologica
Goyal G, Nanduri V.
europepmc   +1 more source

Educational Case: Rosai-Dorfman disease mimicking metastatic carcinoma. [PDF]

Acad Pathol
Rogers M, Danielson DT, Lagerstrom I, Auerbach A.   +3 more
europepmc   +1 more source