RT Journal
A1 Ogbuawa O, Titus-Dillon PY
T1 COngenital adrenal hyperplasia and pseudotumor cerebri
JF Archives of Internal Medicine
JO Archives of Internal Medicine
YR 1979
FD January 1
VO 139
IS 1
SP 120
OP 120
DO 10.1001/archinte.1979.03630380096033
UL http://dx.doi.org/10.1001/archinte.1979.03630380096033
AB To the Editor.— 
    Review of the previous medical literature disclosed no case of congenital adrenal hyperplasia with pseudotumor cerebri. We herein present such a case.Report of a Case.— 
    A 44-year-old woman presented with a four-week history of progressively severe headache, blurred vision, diplopia, and vomiting. She had a 12-year history of hypertension and diabetes mellitus, with a family history for both disorders. Despite continual increase in libido, only one pregnancy occurred 29 years ago. Hirsutism and premenstrual abdominal pain with vomiting have been noted sinced 1958. In 1972, a left tuboovarian abscess was excised. She had previously received psychiatric treatment for depression.Physical examination revealed truncal obesity, facial rounding, and hirsutism. The blood pressure was 180/100 mm Hg.She had frontal hair recession, acne of the face and back, broad shoulders, well-developed breasts, and increased muscle mass of the lower extremities. The pelvis was android, and the clitoris slightly