Results 101 to 110 of about 9,884 (233)

Caso para diagnóstico Case for diagnosis

Anais Brasileiros de Dermatologia, 2011
Relatamos um caso de histiocitose cefálica benigna em uma criança do sexo masculino, de um ano e três meses de idade que desenvolveu múltiplas pápulas na região malar bilateralmente, sem outros comemorativos associados.
Maria de Fátima Guimarães Scotelaro Alves, Carolina Villela da Rocha Miranda, Clarissa de Souza Abreu, Marcela Duarte Villela Benez, Luna Azulay-Abulafia   +4 more
doaj   +1 more source

Colonic Malakoplakia With an Adenomatous Appearance on Magnification Endoscopy: A Case Report

DEN Open, Volume 6, Issue 1, April 2026.
ABSTRACT Malakoplakia is a rare chronic granulomatous disease associated with impaired macrophage phagocytosis of bacteria. Because colonic malakoplakia presents with varied endoscopic appearances, its characteristic features have not been clearly defined, and differentiation from colorectal neoplasms during endoscopy may be difficult. We report a case
Shima Sono, Kiichiro Kaji, Miyabi Miura, Hideo Takayama, Kohei Yasuda, Kuniaki Arai, Kenichi Harada, Shuichi Terasaki   +7 more
wiley   +1 more source

Multiple cutaneous reticulohistiocytoma

Indian Journal of Dermatology, 2016
Multicentric reticulohistiocytosis is a rare non-Langerhans cell histiocytosis characterized in its full form by severe destructive arthritis, cutaneous nodules, and systemic manifestations.
Karishma D Hemmady, Shylaja S Someshwar, Hemangi R Jerajani   +2 more
doaj   +1 more source

Langerhans cell histiocytosis with oral manifestations: a rare and unusual case report [PDF]

, 2012
Langerhans cell histiocytosis (LCH), is a rare, proliferative disorder in which the accumulation of pathologic Langerhans cells leads to local tissue infiltration and destruction.
Agarwal, Manjushree, Rakesh, N., Yashoda Devi, B.K.   +2 more
core   +1 more source

Erdheim‐Chester disease associated with myeloid neoplasm: Clinical features, molecular landscape, and treatment outcomes

HemaSphere, Volume 10, Issue 4, April 2026.
Abstract Erdheim‐Chester disease (ECD) is frequently associated with clonal hematopoiesis and myeloid neoplasms (MN), but clinical phenotype and response to kinase inhibitors (KI) in this setting remain unclear. We analyzed 67 patients with ECD associated with MN (ECD‐MN) from a French national cohort and assessed ECD treatment response, MN progression,
Ambroise Le Pogam, Matthias Papo, Pierre Hirsch, Fleur Cohen‐Aubart, Jean‐François Emile, François Delhommeau, Pierre Duffau, Jérôme Razanamahery, Florence Nguyen‐Khac, Christopher Nunes Gomes, Felicien Triboulet, Jeanne de La Rochefoucauld, Chloé McAvoy, Estibaliz Lazaro, Mehdi Hage‐Sleiman, Damien Roos‐Weil, François Chasset, Vincent Jachiet, Arsène Mekinian, Olivier Fain, Zahir Amoura, Jérôme Hadjadj, Julien Haroche   +22 more
wiley   +1 more source

Baby with neonatal systemic juvenile xanthogranuloma born within a cross-cousin marriage

Dermatologica Sinica, 2015
Juvenile xanthogranuloma is a non-Langerhans cell histiocytosis seen most commonly in childhood and adolescence. Extracutaneous involvement is rare. We report an interesting and extremely rare case of systemic (skin, lung, spleen, and colon) “juvenile ...
Hikmet Tekin Nacaroglu, Demet Can, Canan Sule Unsal Karkiner, Yontem Yaman, Hudaver Alper, Hulya Tosun Yildirim, Paul W. Bishop   +6 more
doaj   +1 more source

Selumetinib as an Effective Therapy of Histiocytic Sarcoma Evolving From a B‐Cell Acute Lymphoblastic Leukaemia

eJHaem, Volume 7, Issue 2, April 2026.
ABSTRACT Introduction Histiocytic sarcoma (HS) is a rare neoplasm derived from non‐Langerhans histiocytic cells, exceptionally arising from B‐ALL. Methods We present the case of a child with high‐risk B‐ALL with PAX5 P80R mutation. Results Despite initial remission, a chemoresistant paravertebral mass was identified as HS.
Laetitia Largeaud, Charlotte Syrykh, Julie Vial, Alban Canali, Isabelle Luquet, François Vergez, Stéphanie Dufrechou, Naïs Prade, André Baruchel, Bastien Gerby, Marie Nolla, Eric Delabesse, Marlène Pasquet   +12 more
wiley   +1 more source

Juvenile Xanthogranuloma: Case Report and Literature Review

International Medical Case Reports Journal, 2020
Sadegh Vahabi-Amlashi, Masoumeh Hoseininezhad, Zahra Tafazzoli Cutaneous Leishmaniasis Research Center, Mashhad University of Medical Sciences, Mashhad, IranCorrespondence: Zahra TafazzoliDepartment of Dermatology, Imam Reza Hospital, Ibn e Sina Street ...
Vahabi-Amlashi S, Hoseininezhad M, Tafazzoli Z   +2 more
doaj  

High Curl Pattern Hair and Scalp Care Considerations to Mitigate Seborrheic Dermatitis

Journal of Cosmetic Dermatology, Volume 25, Issue 4, April 2026.
ABSTRACT Background High‐curl‐pattern hair has unique structural characteristics that increase its susceptibility to breakage and to seborrheic dermatitis (SD). Aims The paper discusses the challenges in effectively treating patients with high‐curl‐pattern hair and SD, and the role of ceramide‐containing products in improving the condition.
Valerie Callender, Cheryl Burgess, Valerie M. Harvey, Candrice Heath, Hope Mitchell, Heather Woolery‐Lloyd, Anneke Andriessen, Amy McMichael   +7 more
wiley   +1 more source

Unique Presentation of Rosai-Dorfman Disease as Concomitant Appendiceal and Rectal Masses with IgG4-Positive Plasma Cells Diagnosed by Core Needle Biopsy

Case Reports in Oncological Medicine, 2020
Rosai-Dorfman disease (RDD), or sinus histiocytosis with massive lymphadenopathy, is a rare non-Langerhans cell histiocytosis. We report a case of a 69-year-old male with concurrent appendiceal and rectal masses who underwent CT-guided percutaneous ...
Jenna J. Poldemann, Benjamin H. Hinrichs, Abouelmagd Makramalla   +2 more
doaj   +1 more source