Restored vision in a young dog following corticosteroid treatment of presumptive hypophysitis [PDF]
, 2016 Background: Hypophysitis is an umbrella term for a group of disorders involving inflammation of the pituitary gland. A rare occurrence in humans, hypophysitis can produce a range of clinical signs including (but not limited to) visual deficits and ...
Liuti, Tiziana +3 more
core +2 more sources
Clinical outcome of a patient with lysosomal acid lipase deficiency and first results after initiation of treatment with Sebelipase alfa: A case report [PDF]
, 2019 We report on a case of very rare autosomal recessive cholesteryl ester storage disease due to lysosomal acid lipase deficiency (LALD). LALD is caused by mutations in the lysosomal acid lipase A (LIPA) gene resulting in cholesteryl ester accumulation in
Bobbert, Thomas +8 more
core +1 more source
Dermatology Online Journal, 2005 A 67-year-old man presented with a 13-year history of slowly enlarging yellow-red plaques on the face and lower extremity. A biopsy specimen was consistent with necrobiotic xanthogranuloma. Necrobiotic xanthogranuloma is a slowly progressive histiocytic disease that is associated with paraproteinemia in most cases; however, its pathogenesis remains ...
Wee, Sue Ann, Shupack, Jerome L
openaire +4 more sources
Xanthogranuloma of Choroid plexus: Case report and Review
Journal of Integrated Health Sciences, 2016 Xanthogranuloma (XG), a condition of obscure pathogenesis and varied terminology, can occur in choroid plexus. We present here xanthogranuloma of the choroid plexus of lateral ventricle, who presented with headache, mild cognitive impairment and ...
D H Bhalodiya +4 more
doaj +1 more source
ADULT ONSET XANTHOGRANULOMA – CASE REPORT AND REVIEW OF LITERATURE [PDF]
Romanian Medical Journal, 2019 Juvenile xanthogranuloma represents the most common form of non-Langerhans cell histiocytosis. It is tipically a childhood disorder, over 80% of cases developing in the first year of life.
Liliana Gabriela Popa +5 more
doaj +1 more source
Xanthogranulomatous hypophysitis: a rare and often mistaken pituitary lesion. [PDF]
, 2015 Xanthogranulomatous hypophysitis (XGH) is a very rare form of pituitary hypophysitis that may present both clinically and radiologically as a neoplastic lesion. It may either be primary with an autoimmune aetiology and can occur in isolation or as a part
Bagga, V. +5 more
core +1 more source
Juvenile xanthogranuloma: clinical-pathological approach. Case reports
Revista de la Facultad de Medicina Humana, 2022 Juvenile Xanthogranuloma is a non-neoplastic skin lesion of the non-Langerhans histiocytosis type, which mainly affects the pediatric population and usually has a self-limited course.
Eugenio A. Palomino Portilla +4 more
doaj +1 more source
Xanthogranulomatous Endometritis in Pregnancy: A Rare Case Concurrent With High-Grade Serous Ovarian Carcinoma. [PDF]
Clin Case RepABSTRACT Xanthogranulomatous endometritis (XGE), typically a postmenopausal condition, has been diagnosed for the first time in a pregnant woman. This case also demonstrates the first reported association of XGE with high‐grade serous ovarian carcinoma, underscoring the need for malignancy screening in XGE patients, regardless of pregnancy status. This
Gogani BS +3 more
europepmc +2 more sources
Xanthogranuloma of the lacrimal sac as a manifestation of Wegener's granulomatosis [PDF]
, 2007 McGill Univ, Ctr Hlth, Dept Ophthalmol & Pathol, Montreal, PQ H3A 2B4, CanadaHenry C Witelson Ocular Pathol Lab, Montreal, PQ, CanadaUniversidade Federal de São Paulo, Dept Ophthalmol, UNIFESP, EPM, São Paulo, BrazilMcGill Univ, Ctr Hlth, Dept Ophthalmol,
A Al-Kandari +8 more
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Neuroendocrine tumor presenting like lymphoma: a case report [PDF]
, 2011 INTRODUCTION: Neuroendocrine tumors are a rare but diverse group of malignancies that arise in a wide range of organ systems, including the mediastinum.
Bruno Beomonte Zobel +6 more
core +2 more sources