Literature DB >> 20048140

Unusual cases of multiple symmetrical lipomatosis with neurological disorders.

Nikolaos I Triantafyllou1, Ioannis Zalonis, Grigoris Kararizos, Konstantinos Gkiatas, Fotini Christidi, Evangelia Kararizou.   

Abstract

Multiple symmetrical lipomatosis (MSL) is a rare disorder of unknown etiology defined as the presence of multiple and symmetrical fatty accumulations, usually involving the upper trunk, neck and head. Frequently associated findings include diabetes mellitus, hyperlipidemia, liver disease, hypothyroidism and polyneuropathy of unknown origin, but nevertheless, there are published reports of cognitive disorders in patients with MSL. We describe two unusual cases (38-year-old and 45-year-old Greek men) of MSL who presented with polyneuropathy and memory disorders. This is the first description of memory disorders in patients with MSL. We propose that Mini-Mental State Examination and assessment of cognitive functions should be performed for all patients with MSL. The underlying mechanism in our patients remains unknown, and this question should be the subject of a future study.

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Year:  2009        PMID: 20048140      PMCID: PMC2801691          DOI: 10.3121/cmr.2009.838

Source DB:  PubMed          Journal:  Clin Med Res        ISSN: 1539-4182


  13 in total

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Journal:  Minerva Med       Date:  1993-03       Impact factor: 4.806

9.  Alcohol consumption, mild cognitive impairment, and progression to dementia.

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Journal:  Muscle Nerve       Date:  1995-07       Impact factor: 3.217

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  2 in total

1.  Case report of comorbid alcohol-induced psychotic disorder and Madelung's disease.

Authors:  Zhenxiao Sun; Huanjun Li
Journal:  Shanghai Arch Psychiatry       Date:  2014-06

2.  Madelung's Disease Leading to Presenile Dementia in a Non-alcoholic Patient.

Authors:  Georges El Hasbani; Richard Assaker; Sutasinee Nithisoontorn; William Plath; Edgardo Olvera Lopez; Jose Vargas Gamarra; Ahmad Kofahi; Christopher Bertely; Vihren Dimitrov
Journal:  Med Arch       Date:  2019-08
  2 in total

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