Zobrazeno 1 - 10
of 982
pro vyhledávání: '"Reticulohistiocytosis"'
Autor:
Surabhi Sudhakaran, Geeta Acharya, Kiran A. Kulkarni, Premalatha T. Siddartha, Vishakha B. Chandrakant, Ramya D. Ravi
Publikováno v:
South Asian Journal of Cancer, Vol 13, Iss 03, Pp 185-190 (2024)
Externí odkaz:
https://doaj.org/article/3c5d16f2eb314f0888cda564f80c0547
Autor:
Tian Ran Zhu, MD, Diana Zarowin, BS, Adnan Mir, MD, PhD, Julia Gittler, MD, Caroline Halverstam, MD
Publikováno v:
JAAD Case Reports, Vol 48, Iss , Pp 144-147 (2024)
Externí odkaz:
https://doaj.org/article/8957ed6bfd1d46cc9b34efb4da1164d1
Publikováno v:
Medwave, Vol 24, Iss 05, Pp e2914-e2914 (2024)
Multicentric reticulohistiocytosis is a rare non-Langerhans cell histiocytosis of unknown etiology. It is classified as multicentric because of multisystem involvement. The disease predominantly affects the skin and joints, but visceral involvement i
Externí odkaz:
https://doaj.org/article/cb4790d702834f66afd095ffc7e20923
Autor:
Daniel Gonzalez, Vinh Lu, Madeline Bonnet, Rachelle Gietzen, Anthony Linfante, Enrique Medina, Vijaya Murthy
Publikováno v:
Rheumatology & Autoimmunity, Vol 3, Iss 3, Pp 179-184 (2023)
Abstract Introduction Multicentric reticulohistiocytosis (MRH) is a rare disease that is known to affect the skin and joints, primarily. It is considered a rare form of non‐Langerhans cell histiocytosis (Group C) that can cause destructive inflamma
Externí odkaz:
https://doaj.org/article/1162813c21f44e3ba9a4fb46a5b5466b
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Multicentric reticulohistiocytosis (MRH) is a rare systemic disorder characterized by histiocytic hyperplasia that mainly involves the skin, mucous membranes, and joints. The typical clinical features include papules, nodules, and arthritis. MRH lesi
Externí odkaz:
https://doaj.org/article/202abd4e3310499baa34c2db5174563d
Autor:
Colin M. Kincaid, BS, Ajay N. Sharma, MD, Justin D. Arnold, MD, Luke Horton, MD, Bonnie A. Lee, MD, Natasha A. Mesinkovska, MD, PhD
Publikováno v:
JAAD Case Reports, Vol 33, Iss , Pp 73-76 (2023)
Externí odkaz:
https://doaj.org/article/fd83130e794b4f1d8f7c70640895f70d
Publikováno v:
Case Reports in Dermatology, Vol 15, Iss 1, Pp 10-16 (2023)
Multicentric reticulohistiocytosis (MRH) is categorized as a rare non-Langerhans cell histiocytosis most commonly seen in women in the fourth to fifth decade of life. This systemic inflammatory condition affects multiple organ systems and can result
Externí odkaz:
https://doaj.org/article/7f1c2e2f4d444379af57f050c87258ec
Publikováno v:
Clinical Case Reports, Vol 11, Iss 9, Pp n/a-n/a (2023)
Key Clinical Message Multicentric reticulohistiocytosis is a rare multisystemic condition associated with papulonodular skin lesions, severe arthritis and malignancy. Histopathology shows histiocytes containing abundant eosinophilic ground glass cyto
Externí odkaz:
https://doaj.org/article/c69a597775ac4009a960b22abec2189d
Autor:
Xiao-juan Zou, Lin Qiao, Feng Li, Hua Chen, Yun-jiao Yang, Dong Xu, Wen-Jie Zheng, Zhen-yu Jiang, Li Wang, Qing-jun Wu, Feng-Chun Zhang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-9 (2022)
Abstract Objective To investigate the clinical features of multicentric reticulohistiocytosis (MRH). Methods The clinical manifestations, laboratory examination results and histologic characteristics of eleven patients with MRH were collected and com
Externí odkaz:
https://doaj.org/article/df5b6fc9ef8640a3aeb4c8637907df9f
Autor:
Alessandra Rizzoli, Simona Giancristoforo, Cristina Haass, Rita De Vito, Stefania Gaspari, Eleonora Scapillati, Andrea Diociaiuti, May El Hachem
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-4 (2021)
Abstract Background Congenital self-healing reticulohistiocytosis (CSHRH), also called Hashimoto-Pritzker disease, is a rare and benign variant of Langerhans cell histiocytosis, characterized by cutaneous lesions without extracutaneous involvement. C
Externí odkaz:
https://doaj.org/article/038fa595abb4487aba2be59d442c9c05