Literature DB >> 12493122

Diencephalic syndrome of emaciation in an adult associated with a third ventricle intrinsic craniopharyngioma: case report.

Yasuyuki Miyoshi1, Masatoshi Yunoki, Akimasa Yano, Ken Nishimoto.   

Abstract

OBJECTIVE AND IMPORTANCE: Diencephalic syndrome of emaciation (DS) is seen almost exclusively in infants and young children, and only two cases of DS in adults have been reported previously. We describe a case of DS associated with a third ventricle intrinsic craniopharyngioma in an adult patient. CLINICAL
PRESENTATION: A 54-year-old man presented with profound emaciation, disorientation, memory loss, and psychological disorders. Computed tomographic scanning and magnetic resonance imaging of his brain disclosed a tumor within the third ventricle. The preoperative endocrinological examination indicated an elevated growth hormone level and a decreased somatomedin C level. INTERVENTION: The patient underwent partial resection of the tumor, which was adherent to the floor of the third ventricle but not to the ventricle wall, by an interhemispheric-transcallosal approach. The histological examination revealed a squamous papillary-type craniopharyngioma. The patient received 50 Gy of radiotherapy, which resulted in 90 to 95% reduction of the tumor size within 6 months, as indicated by the magnetic resonance images presented. The psychological disorders, memory disturbance, and severe emaciation improved gradually thereafter.
CONCLUSION: Although extremely rare, DS can occur in an adult harboring a tumor in the anterior hypothalamus.

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Year:  2003        PMID: 12493122     DOI: 10.1097/00006123-200301000-00029

Source DB:  PubMed          Journal:  Neurosurgery        ISSN: 0148-396X            Impact factor:   4.654


  2 in total

1.  Lymphomatosis cerebri presenting with orthostatic hypotension, anorexia, and paraparesis.

Authors:  Anjeni Keswani; Eileen Bigio; Sean Grimm
Journal:  J Neurooncol       Date:  2012-07-18       Impact factor: 4.130

2.  Diencephalic syndrome as sign of tumor progression in a child with neurofibromatosis type 1 and optic pathway glioma: a case report.

Authors:  Maria Elena Cavicchiolo; Enrico Opocher; Marco Daverio; Matteo Bendini; Elisabetta Viscardi; Gianni Bisogno; Giorgio Perilongo; Liviana Da Dalt
Journal:  Childs Nerv Syst       Date:  2013-04-25       Impact factor: 1.475

  2 in total

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