A diagnosis not to miss: Pheochromocytoma during pregnancy [8]

Journal of Neurology

Volumn 254, Issue 11, 2007, Pages 1612-1613

  Kondziella, D ^a   Lycke, J ^a   Szentgyorgyi E ^a  

^a SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CASE REPORT; CESAREAN SECTION; CHROMAFFIN CELL; CHROMOSOME 10Q; CHROMOSOME 17Q; DIAGNOSTIC TEST; FEMALE; GENE MUTATION; HUMAN; LABORATORY TEST; LETTER; LUMBAR PUNCTURE; MAGNETIC RESONANCE ANGIOGRAPHY; MATERNAL MORTALITY; MICROSCOPY; NEUROIMAGING; NEUROLOGIC EXAMINATION; OPHTHALMOSCOPY; PHEOCHROMOCYTOMA; PREGNANT WOMAN; PREVALENCE; PRIORITY JOURNAL; SYMPTOMATOLOGY;

ADULT; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; PHEOCHROMOCYTOMA; PREGNANCY; TOMOGRAPHY, X-RAY COMPUTED;

EID: 36348981033     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-007-0605-9     Document Type: Letter

References (6)

1. Manger WM (2006) An overview of pheochromocytoma. History, current concepts, vagaries, and diagnostic challenges. Ann NY Acad Sci 1073:1-20
2. Hudsmith JG, Thomas CE, Browne DA (2006) Undiagnosed pheochromocytoma mimicking severe preeclampsia in a pregnant woman at term. Int J Obstet Anesthesia 15:240-245
3. Ahlawat SK, Jain S, Kumari S, Varma S, Sharma BK (1999) Pheochromocytoma associated with pregnancy: case report and review of the literature. Obstet Gynecol Surv 54:728-737
4. Manger M (2005) The vagaries of pheochromocytoma. Am J Hypertens 18:1266-1270
5. Neumann HPH, Bausch B, McWhinney SR, Bender BU, Gimm O, Franke G, Schipper J, Klisch J, Altehoefer C, Zerres K, Januszewicz A, Eng C (2002) Germline mutations in nonsyndromic pheochromocytoma. N Engl J Med 346:1459-1466
6. Ellison GT, Mansberger JA, Mansberger AR Jr (1988) Malignant recurrent pheochromocytoma during pregnancy. Surgery 103:484-489