Results 21 to 30 of about 14,015 (245)

Erdheim–Chester Disease of the Breast: First Review and First Case of Isolated Severe Gynecomastia

Diagnostics, 2023
(1) Introduction: Erdheim–Chester disease (ECD) is a life-threatening condition and often a diagnostic challenge. It has recently been classified as a hematopoietic tumour, and the cases of ECD reported in the literature has dramatically increased during
Francesco Ruben Giardino, Roberto Cuomo, Mirco Pozzi, Gianluca Marcaccini, Stefano Bacchini, Mohamed Marzouk El Araby, Luca Grimaldi, Giuseppe Nisi   +7 more
doaj   +1 more source

Langerhans cell histiocytosis presenting as eosinophilic granuloma of the bilateral forearms in an 8-year-old girl: a case report

Journal of Medical Case Reports, 2019
Background Langerhans cell histiocytosis previously known as histiocytosis X is a rare disease of children and young adults with a very broad clinical spectrum. In children, its annual incidence is estimated between 0.2–0.5 per 100,000.
Salahoudine Idrissa, Hind Cherrabi, Boubacar Efared, Kassim Sidibé, Karima Attaraf, Lamiae Chater, Abderahmane Afifi   +6 more
doaj   +1 more source

HYSTYOCYTOSIS X: VERIFICATION OF DIAGNOSIS

Vestnik Dermatologii i Venerologii, 2018
A clinical case of histiocytosis X, rarely found in the practice of a dermatovenereologist, is described, the pathognomonic clinical symptoms of this dermatosis, including skin lesions, that occur in 50 to 80 % of cases of all forms are displayed.
V. V. Starostenko, L. A. Anisimova, O. A. Sidorenko, E. P. Opruzhenkova   +3 more
doaj   +1 more source

Choroidal Neovascular Membrane Formation and Retinochoroidopathy in a Patient with Systemic Langerhans Cell Histiocytosis: A Case Report and Review of the Literature [PDF]

, 2012
We report a case of bilateral atrophic retinochoroidopathy with choroidal neovascular membrane (CNVM) formation in a patient with systemic Langerhans cell histiocytosis (LCH).
Foster, Charles Stephen, Thanos, Aristomenis, Vavvas, Demetrios, Young, Lucy Hwa-Yue   +3 more
core   +2 more sources

Langerhans´cell histiocytosis [PDF]

, 2014
La histiocitosis de células de Langerhans (HCL), anteriormente conocida como histiocitosis X, es una enfermedad poco frecuente caracterizada por la acumulación y proliferación de histiocitos, eosinófilos y células de Langerhans, con inclusión de gránulos
Casanovas, A., Elena, G., Rosso, Diego
core   +1 more source

A rare case of oral multisystem Langerhans cell histiocytosis [PDF]

, 2017
Langerhans cell histiocytosis (LCH) is a rare disorder characterized by high proliferation of Langerhans dendritic cells. LCH is a solitary or multifocal disease that primarily involves bone tissue and often affects children and young men. A 29 years-old
Facciolo, Maria Teresa, Gaglioti, Domenico, Gallenzi, Patrizia, Patini, Romeo, Riva, Francesco   +4 more
core   +1 more source

Vulvar Langerhans cell histiocytosis: a case report

The Pan African Medical Journal, 2014
Langerhans cell histiocytoses (LCH) are a rare group of disorders that comprise a large spectrum of diseases initially known as histiocytosis X. In this case report, we relate a case of LCH affecting the vulva of a 47-year-old female.
Nadia Khoummane, Cyriane Guimeya, Dominique Lipombi, Franeois Gielen   +3 more
doaj   +1 more source

Growth of children with Langerhans cell histiocytosis [PDF]

, 1995
Conclusion: GH deficiency is not a common manifestation of LCH in childhood and GH provocation tests are only indicated when there is a poor or decelerating growth rate.
Egeler, R.M. (Maarten), Hoek, A.C.J. (A. C J) van den, Hählen, K. (Karel), Karstens, A. (A.)   +3 more
core   +1 more source

Orbital involvement in Rosai-Dorfman disease [PDF]

, 2011
A doença de Rosai-Dorfman (DRD) ou histiocitose sinusal com linfadenopatia maciça é uma entidade clínica idiopática, rara e benigna, caracterizada pela proliferação histiocitária com linfofagocitose. Geralmente se apresenta com linfoadenomegalia cervical,
GONÇALVES, Allan C. Pieroni, MONTEIRO, Mário Luiz Ribeiro, MOURA, Frederico Castelo, OLIVEIRA, Cristiana Dumaresq de, Rossato, Luiz Angelo   +4 more
core   +2 more sources

Langerhans cell histiocytosis in an adult with oral cavity involvement: Posing a diagnostic challenge

Contemporary Clinical Dentistry, 2019
Langerhans cell histiocytosis (LCH) is a rare hematological disorder characterized by local or generalized, uncontrolled proliferation and infiltration of Langerhans type of histiocytic cells.
Richa Nangalia, Rudra Prasad Chatterjee, Sanchita Kundu, Mousumi Pal   +3 more
doaj   +1 more source