Systemic findings of Langerhans cell histiocytosis in neonatal period
Revista de la Facultad de Ciencias de la Salud, 2011 We report an unusual case of mediastinal abcessed mass, with involvement of the lung, thymus and probably bone and hematopoietic system, in a newborn that was diagnosed with Langerhans cell histiocytosis.
Rosalba Días-Castro +6 more
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Rare Tumors, 2011 We present a patient (50-year-old male) with coexisting Warthin tumor and involvement of two intraparotid lymph nodes by Langerhans cell histiocytosis associated with necrosis, eosinophilic abscesses and a granulomatous reaction.
Char Loo Tan +2 more
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Histiocitosis de células de Langerhans en el raquis infantil [PDF]
, 2006 Introducción: la Histiocitosis de células de Langerhans incluye un amplio espectro de enfermedades de etiología desconocida, observada preponderantemente en niños.
Fernández, Claudio A. +2 more
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A Case of Refractory Langerhans Cell Histiocytosis Complicated with Hemophagocytic Lymphohistiocytosis Rescued by Cord Blood Transplantation with Reduced-intensity Conditioning [PDF]
, 2017 We diagnosed a female infant with Langerhans cell histiocytosis (LCH) who was refractory to conventional chemotherapy. She showed refractory inflammation that was complicated with hemophagocytic lymphohistiocytosis (HLH) during LCH chemotherapy ...
Kanamitsu, Kiichiro +4 more
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Langerhans’ cell histiocytosis diagnosed due to dermatological perianal lesion
Journal of Coloproctology, 2017 Langerhans’ cell histiocytosis is a rare disease characterized by proliferation of Langerhans cells in the body. It affects mainly males, predominantly in childhood. Ulcerated plaques are one of the cutaneous forms of presentation.
Bruno Lorenzo Scolaro +5 more
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Histiocytosis X: Langerhans’ Cell Histiocytosis
Hematology/Oncology Clinics of North America, 1987 Histiocytosis X is a complex and poorly understood entity. Nevertheless, it would appear as if certain themes are found recurrently throughout the literature dealing with this disease and a review of them serves as a useful summary. 1. Problems with Nomenclature.
openaire +2 more sources
Langerhans Cell Histiocytosis of the Clavicle in a 13-Year-Old Boy
Case Reports in Orthopedics, 2014 Langerhans Cell Histiocytosis (LCH) is a rare neoplasm characterized by abnormal proliferation of histiocytic cells. In this case report, we describe a unique case of a 13-year-old boy who presented to the clinic with an insidious onset of mid-clavicular
Shital N. Parikh +3 more
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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 +5 more
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Langerhans' cell histiocytosis of the temporal bone in an adult with central diabetes insipidus
Radiology Case Reports, 2019 We present a case of Langerhans’ cell histiocytosis in a 40-year-old woman presenting with central diabetes insipidus and right ear pain. As this disease process is often clinically challenging, the presence of certain imaging findings should raise the ...
Amanda Allen, DO +5 more
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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 +2 more
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