Results 91 to 100 of about 17,930 (201)

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

Perifollicular Langerhans cell histiocytosis

Dermatology Online Journal, 2012
A 25-year-old man presented with a 13-year history of an erythematous, papular eruption of his face and trunk, which was treated in the past as acne and psoriasis with isotretinoin and methotrexate, respectively. Histopathologic examination demonstrated an infiltrate of Langerhans cells, which was consistent with Langerhans cell histiocytosis.
Mir, Adnan, Fisher, Max, Kamino, Hideko, Soter, Nicholas A   +3 more
openaire   +4 more sources

Polyostotic Langerhans cell histiocytosis presenting as halitosis in a 24-year-old man: a case report

Journal of Medical Case Reports
Background Langerhans cell histiocytosis is a rare disease of the reticuloendothelial system. This report presents a novel case of Langerhans cell histiocytosis with systemic involvement that started with a simple chief complaint.
Hassan Mirmohammad Sadeghi, Sanaz Gholami Toghchi, Fatemeh Mashhadiabbas, Milad Baseri, Maryam Mohammadalizadeh Chafjiri, Parnian Nikraftar, Ardeshir Khorsand   +6 more
doaj   +1 more source

A neonatal pustule:Langerhans cell histiocytosis [PDF]

, 2019
Langerhans cell histiocytosis (LCH) is a rare, clinically heterogeneous disease that most commonly occurs in pediatric populations. Congenital self-limited LCH is a benign variant of LCH.
Hogeling, Marcia, Kang, Yuna, Knowles, Byron, McKenzie, Shanice, Vecerek, Natalia   +4 more
core  

Bagaimana Prognosis Histiocytosis? Sebuah Laporan Kasus [PDF]

, 2013
Penderita histiocytosis dengan keterlibatan multiorgan dan disertai gangguan fungsi organ mempunyai prognosis buruk dan tingkat mortalitas tinggi. Dilaporkan seorang penderita histiocytosis, usia 1 tahun 1 bulan yang datang dengan kelainan di kulit ...
Lestari, R. D. (Rini), Mulatsih, S. (Sri)   +1 more
core  

Primary oral manifestation of Langerhans cell histiocytosis refractory to conventional therapy but susceptible to BRAF-specific treatment: a case report and review of the literature [PDF]

, 2019
Langerhans cell histiocytosis (LCH) is a diagnostic and therapeutic challenge. We report on a rare case of its primary oral manifestation that was treated successfully with the BRAF-specific agent, vemurafenib, after insufficient standard LCH treatment ...
Beck-Broichsitter, Benedicta, Doueiri, Mohemed-Salim, Heiland, Max, Lissat, Andrej, Neckel, Norbert, Raguse, Jan-Dirk, Spors, Birgit, Stackelberg, Arendt von, Thieme, Nadine   +8 more
core   +1 more source

Langerhans cell histiocytosis: Two clinical presentations in the same patient [PDF]

, 2012
Langerhans cell histiocytosis (LCH) is a heterogeneous group of diseases characterized by a pathological proliferation of cells phenotypically similar to Langerhans cells.
Lobo, I., Machado, S., Oliveira, A., Pinto-Almeida, T., Selores, M.   +4 more
core   +1 more source

Erdheim Chester disease – 25 year history with early CNS involvement [PDF]

, 2016
We report a case of Erdheim-Chester disease (ECD) with a 25-year history following initial presentation with diabetes insipidus and brainstem involvement.
Cohen, N, Hall, C A, McCoubrie, Paul, Renowden, S, Rice, Claire, Scolding, Neil   +5 more
core   +2 more sources

رتيکولوهيستيوسيتوز خود محدود شونده مادرزادی (گزارش 1 مورد با ضايعه منفرد) [PDF]

, 2004
رتيکولوهيستيوسيتوز خود محدود شونده مادرزادی نوعی هيستيوسيتوز سلول لانگرهانس می‌باشد که پاتوفيزيولوژی و عامل آن به خوبی مشخص نشده است. برخی از مولفان مکانيسم‌های ايمنی‌ که موجب افزايش توليد سيتوکين‌ها می‌شوند را در ايجاد آن موثر می‌دانند.
ارجمندی رفسنجانی, خدیجه, مهرآزما, میترا, وثوق, پروانه   +2 more
core  

Case series of volar juvenile xanthogranuloma: Clinical observation of a peripheral rim of hyperkeratosis [PDF]

, 2014
Juvenile xanthogranuloma is a benign histiocytic tumor predominantly occurring in children as yellowish papules on the head and trunk. Presentations on the volar surfaces are rare and may cause diagnostic confusion with pyogenic granuloma, eccrine poroma
Amadi, Ugochukwu, Do, Thy Thy, Ha Lan, Thanh T., Hristov, Alexandra, Khandpur, Ritika, Maier, Lisa, Mervak, Julie, Wang, Frank   +7 more
core   +1 more source