Literature DB >> 21305332

Exophytic hypothalamic cavernous malformation mimicking an extra-axial suprasellar mass.

Matt Rheinboldt1, John Blase.   

Abstract

We report the case of a 31-year-old male who presented to the ER with a 1-week history of progressively worsening, throbbing, left retro-orbital headache, ptosis, and subjective worsening of short-term memory function. Initial review of systems and laboratory data were noncontributory. Non-contrasted CT demonstrated a large hyperdense mass centered in the suprasellar cistern without evidence of dissecting extra-axial hemorrhage. Though the initial appearance mimicked a basilar tip aneurysm or another primary extra-axial suprasellar pathology such as a hemorrhagic or proteinaceous craniopharyngioma, germinoma, or optic glioma, a second smaller, clearly intra-axial, hyperdense lesion was observed in the left periventricular forceps major white matter. Consideration for multiple cavernomas versus hypervascular metastatic disease such as renal malignancy, thyroid malignancy, or melanoma was raised. CTA confirmed normal intracranial vasculature. Subsequent MRI images showed an acutely hemorrhagic mass centered at the left paramedian hypothalamus and tuber cinereum with numerous secondary foci, demonstrating mature hemorrhagic elements and confirming the diagnosis of multiple cavernomas.

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Year:  2011        PMID: 21305332     DOI: 10.1007/s10140-011-0940-0

Source DB:  PubMed          Journal:  Emerg Radiol        ISSN: 1070-3004


  16 in total

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2.  Cavernous malformation of the optic nerve mimicking optic neuritis.

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3.  The MRI appearance of cavernous malformations (angiomas).

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4.  Multiple cerebral and spinal cord cavernomas in Klippel-Trenaunay-Weber syndrome.

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Journal:  J Clin Neurosci       Date:  2010-05-20       Impact factor: 1.961

Review 5.  Emerging clinical imaging techniques for cerebral cavernous malformations: a systematic review.

Authors:  Peter G Campbell; Pascal Jabbour; Sanjay Yadla; Issam A Awad
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6.  Familial versus sporadic cavernous malformations: differences in developmental venous anomaly association and lesion phenotype.

Authors:  T A Petersen; L A Morrison; R M Schrader; B L Hart
Journal:  AJNR Am J Neuroradiol       Date:  2009-10-15       Impact factor: 3.825

7.  Management of pediatric brainstem cavernous malformations: experience over 20 years at the hospital for sick children.

Authors:  Ratan D Bhardwaj; Kurtis I Auguste; Abhaya V Kulkarni; Peter B Dirks; James M Drake; James T Rutka
Journal:  J Neurosurg Pediatr       Date:  2009-11       Impact factor: 2.375

8.  Susceptibility-weighted imaging for the evaluation of patients with familial cerebral cavernous malformations: a comparison with t2-weighted fast spin-echo and gradient-echo sequences.

Authors:  J M de Souza; R C Domingues; L C H Cruz; F S Domingues; T Iasbeck; E L Gasparetto
Journal:  AJNR Am J Neuroradiol       Date:  2007-10-18       Impact factor: 3.825

9.  Surgical management of brain-stem cavernous malformations: report of 137 cases.

Authors:  Chung-cheng Wang; Ali Liu; Jun-ting Zhang; Bo Sun; Yuan-li Zhao
Journal:  Surg Neurol       Date:  2003-06

10.  The natural history of familial cavernous malformations: results of an ongoing study.

Authors:  J M Zabramski; T M Wascher; R F Spetzler; B Johnson; J Golfinos; B P Drayer; B Brown; D Rigamonti; G Brown
Journal:  J Neurosurg       Date:  1994-03       Impact factor: 5.115

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  3 in total

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2.  Optic chiasmal cavernous angioma: A rare suprasellar vascular malformation.

Authors:  Hussam Abou-Al-Shaar; Ayman Bahatheq; Radwan Takroni; Ibrahim Al-Thubaiti
Journal:  Surg Neurol Int       Date:  2016-08-01

3.  Hypothalamic Cavernous Malformation: Surgical Technique and Literature Review.

Authors:  Nataly Alvear-Quito; Alejandro Ceja-Espinosa; Juan P Navarro-Garcia de Llano; Aurelio Ponce-Ayala; Edgar Nathal
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  3 in total

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