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. +4 more
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Clinicopathological characteristics of histiocytic sarcoma affecting the central nervous system in dogs. [PDF]
, 2020 BackgroundHistiocytic sarcoma affecting the central nervous system (CNS HS) in dogs may present as primary or disseminated disease, often characterized by inflammation.
Crowe, Chelsea M +10 more
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Orthotopic liver transplantation in children. Two-year experience with 47 patients [PDF]
, 1984 During a 24-month period (May 1981 to May 1983), 47 pediatric patients (ranging in age from 7 months to 18 years) underwent orthotopic liver transplantation using cyclosporine and prednisone.
Gartner, JC +5 more
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Successful Treatment of Paediatric Necrobiosis Lipoidica With Baricitinib
JEADV Clinical Practice, EarlyView.ABSTRACT Necrobiosis lipoidica (NL) is a rare, chronic granulomatous condition that typically presents as sharply demarcated plaques with telangiectasia and atrophic centres. Paediatric cases are uncommon, and treatment options often fail to address refractory cases.
P. Simões Farinha, M. J. Paiva‐Lopes
wiley +1 more source
histiocytic Necrotizing Lymphadenitis
Apollo Medicine, 2006 We are presenting a case of histiocytic necrotizing lymphadenitis (Kikuchi disease), which is characterized by involvement of lymph nodes, skin, liver and spleen. A 21-year-old girl presented with 27 days history of prolonged fever, left cervical painless lymphadenitis and maculo-papular skin rashes.
Vijay Kumar Aneja +2 more
openaire +2 more sources
Primary Head and Neck Histiocytic Sarcoma of the Oropharyngeal Posterolateral Wall: A Case Report
The Laryngoscope, EarlyView.Histiocytic sarcoma (HS) is a rare and aggressive malignancy, particularly uncommon in the head and neck region. This report describes the case of a 67‐year‐old male with HS originating from the oropharyngeal posterolateral wall, treated successfully with transoral CO2 laser excision and adjuvant proton radiotherapy.
Michael Dalè +8 more
wiley +1 more source
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 +8 more
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Molecular Nutrition &Food Research, EarlyView.This study compared the preventive effects of dietary resistant starch (RS2) from maize and d‐fagomine (FG) from buckwheat on cardiometabolic risk factors in high‐fat (HF) diet‐fed rats. Wistar‐Kyoto rats (n = 11–12/group) received STD, HF, HF + RS, or HF + FG diets for 10 weeks.
Bernat Miralles‐Pérez +10 more
wiley +1 more source
Frontiers in Oncology, 2020 Central nervous system involvement in Hodgkin lymphoma is extremely rare, especially in nodular lymphocyte predominant Hodgkin lymphoma (NLPHL), which usually carries a favorable prognosis.
Paolo Salvioni Chiabotti +9 more
doaj +1 more source
Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in a ten-year-old girl accompanied by posterior reversible encephalopathy syndrome and disseminated herpes simplex virus infection [PDF]
, 2015 可逆性後頭葉白質脳症は通常臨床的には頭痛・痙攣・視覚障害等の神経症状で発症するしばしば認める疾患である．一方，播種性ヘルペス感染症は免疫不全患者で認める感染症である．今回我々は，EBウイルス関連血球貪食症候群に対するエトポシド・プレドニゾロン・シクロスポリンを用いた多剤併用化学療法中に，シクロスポリン関連可逆性後頭葉白質脳症と播種性ヘルペス感染症と診断された10歳女児を経験したので報告する．EBウイルス関連血球貪食症候群に対する併用療法は当初有効であったが ...
板倉 隆太 +5 more
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