Progression of neurovisceral storage disease with supranuclear ophthalmoplegia following orthotopic liver transplantation [PDF]
, 1986 A 7-year-old girl with progressive ataxia, spasticity, supranuclear ophthalmoplegia, and sea-blue histiocytes in her bone marrow underwent orthotopic liver transplantation for hepatocellular carcinoma.
Bergman, I +8 more
core
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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A Rare Case of Primary Intraparenchymal Rosai‐Dorfman Disease
iRADIOLOGY, EarlyView.
Lin Chen, Rui Zhou
wiley +1 more source
Veterinary Record Case Reports, EarlyView.Abstract This report describes a case of refractory ionised hypercalcaemia, of 12 months duration, in an 11‐year‐old, male, neutered beagle diagnosed with metastatic histiocytic sarcoma at postmortem examination. In this case, the parathyroid hormone levels were at the lower end of the reference interval, the parathyroid hormone‐related peptide was ...
Kerry E. Rolph +5 more
wiley +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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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
core +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
British Journal of Haematology, EarlyView.The international prognostic index (IPI)‐driven trial inclusion criteria may have contributed to the failure of some of the first‐line trials in large B‐cell lymphoma (LBCL). GLA and LYSA collaborated to improve prognostic stratification in LBCL by analyzing data from trial cohorts and proposed the smIPI.
Umut Yılmaz +24 more
wiley +1 more source
Rosai-Dorfman disease with spontaneous resolution: case report of a child
Revista Brasileira de Hematologia e Hemoterapia, 2011 Rosai-Dorfman disease is a self-limiting condition caused by histiocyte proliferation within the sinusoids of lymph nodes and in extranodal tissue. It is a rare disease, particularly in children, that progresses with extensive lymphadenopathy. This paper
Felipe Barbosa Lima +4 more
doaj +1 more source