Results 51 to 60 of about 20,564 (250)

An unusual unifocal presentation of Castleman’s disease in a young woman with a detailed description of sonographic findings to reduce diagnostic uncertainty: a case report [PDF]

, 2013
Background: Castleman’s disease is a rare lymphoproliferative disorder. It typically presents as mediastinal masses and causes a wide range of clinical symptoms.
Maden, Zerrin, Wagner, Norbert
core   +1 more source

Studying Cat (Felis catus) Diabetes: Beware of the Acromegalic Imposter [PDF]

, 2015
Naturally occurring diabetes mellitus (DM) is common in domestic cats (Felis catus). It has been proposed as a model for human Type 2 DM given many shared features.
AC Dirtu, AF Daly, AL Prahl, Andrew Wolfe, CC Capen, CE Reusch, Christopher R. Lamb, CR Lamb, David B. Church, E Resmini, ED Aflorei, H Biering, JD Nabarro, JWM Höppener, Ken Smith, KH Johnson, M Hoenig, M Hoenig, M Scacchi, MJ Brearley, MO Thorner, MS Lewitt, Márta Korbonits, N Alt, N Kokka, Norelene Harrington, O Alexopoulou, Panagiotis Mantis, PI Shishko, PJ Kenny, PW Rosario, R Gostelow, R Lederer, R Tyson, Rob Fowkes, S Melmed, SJ Niessen, SJ Niessen, SJ Niessen, SJ Niessen, Stijn J. M. Niessen, TD O'Brien, TM McCann, Y Forcada, Yaiza Forcada   +44 more
core   +3 more sources

The first case of thrombocytopenia, anasarca, fever, renal impairment or reticulin fibrosis, and organomegaly (TAFRO) syndrome with unilateral adrenal necrosis: a case report

Journal of Medical Case Reports, 2018
BackgroundTAFRO syndrome, which was first reported in 2010 in Japan, is a relatively rare disease characterized by thrombocytopenia, anasarca, fever, renal impairment, reticulin fibrosis, and organomegaly.
Y. Fujiwara, Kana Ito, A. Takamura, K. Nagata   +3 more
semanticscholar   +1 more source

An intriguing autopsy case of gangrene intestine [PDF]

, 2006
Background Hashimoto’s thyroiditis is one of the most common causes of hypothyroidism. Hypothyroidism is a known cause of hyperlipidemia. There is a strong correlation between coronary and mesenteric vessel atherosclerosis.
E., E.Jayashankar, Patnayak, Rashmi Patnayak, Prayaga, Aruna K. Prayaga, Reddy, Rajasekhar Reddy, S.V.N., S.V.N. Anuradha   +4 more
core   +2 more sources

Baricitinib treatment for refractory skin changes in POEMS syndrome: a case report

Frontiers in Pharmacology, 2023
Polyneuropathy, organomegaly, endocrinopathy, monoclonal plasma cell disorder, and skin changes (POEMS) syndrome is a multisystem disorder that has limited treatment options.
Jingjing Xie, Jingjing Xie, Zhiling Li, Yubao Jiang, Yubao Jiang, Dabin Tang, Dabin Tang, Xia Qiu, Xia Qiu, Ertao Jia, Ertao Jia, Jianyong Zhang, Jianyong Zhang   +12 more
doaj   +1 more source

POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes)

Dermatology Online Journal, 2009
A 62-year-old woman with hypothyroidism presented with a seven-year history of paresthesias, itching, and edema of the skin. Physical examination showed indurated, edematous plaques on the lower extremities. A biopsy specimen showed increased mucin deposition that was consistent with myxedema, and monoclonal IgM was observed on immunofixation.
Liang, Christine, Gonzalez, Mercedes, Patel, Rishi, Meehan, Shane, Kamino, Hideko, Jr, Andrew G Franks   +5 more
openaire   +4 more sources

Monomorphic type of maculopapular cutaneous mastocytosis: rationale for interdisciplinary collaboration

Онкогематология
Backround. Mastocytosis is a rare disease characterized by pathological accumulation of mast cells in one or more organs. According to the world Health Organization classification (2016), a monomorphic type of maculopapular cutaneous mastocytosis ...
E. I. Kasikhina, N. N. Potekaev, O. V. Zhukova, M. N. Ostretsova   +3 more
doaj   +1 more source

Castleman disease of the hyaline vascular variant transforming to POEMS syndrome as endpoint: a case report

BMC Neurology, 2018
Background POEMS syndrome is a rare neoplastic syndrome reflected by plasma cell disorder. It is composed by polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes. It is also reported to associate with Castleman disease.
Yijun Ge, Qian Da, Ying Dai
doaj   +1 more source

Nutritional Potential, Phytochemical Content, In Vivo Antioxidant, and Antanemic Potential of Musa paradisiaca Flower

Food Chemistry International, EarlyView.
After collecting Musa paradisiaca leaves, some were dried and others were used to produce aqueous extracts. The extracts and powders were characterized and then administered to rats made anaemic by PHZ. After 14 days of administration of the two samples, the rats were euthanized and it was observed that after 9 days of treatment, the aqueous extract ...
Josée Rebeca Nombo, Jethro Roland Misse Ngangue Ekwala, Somon Régine Tuem, Stéphano Tene Tambo, Merlin Ngafon Nchoutpouen, Valery Jean François Nsoga, Jules Christophe Koule Manz, Jordan Mekui Nwotue, Mathieu Ndomou   +8 more
wiley   +1 more source

Rapunzel syndrome: Trichobezoar‐induced pancreatitis unraveled

JPGN Reports, EarlyView.
Abstract Trichobezoars are rare hair‐based intraluminal foreign bodies that may cause significant gastrointestinal complications, particularly when extending into the duodenum as in Rapunzel syndrome. We report the case of an 11‐year‐old girl with sensory processing difficulties and undiagnosed avoidant/restrictive food intake disorder (ARFID), who ...
Halen Scott, Alisha Sansguiri, Ashley Polachek, Stacy Matthews, Megha Mehta   +4 more
wiley   +1 more source