PSEUDOTUMORAL LYMPHOCYTIC HYPOPHYSITIS SUCCESSFULLY TREATED BY CORTICOSTEROID ALONE - FIRST CASE-REPORT

被引:76
作者
BERESSI, N
COHEN, R
BERESSI, JP
DUMAS, JL
LEGRAND, M
IBAZIZEN, MT
MODIGLIANI, E
机构
[1] HOP AVICENNE,DEPT ENDOCRINOL,F-93009 BOBIGNY,FRANCE
[2] HOP AVICENNE,DEPT RADIOL,F-93009 BOBIGNY,FRANCE
[3] HOP 15 20,PARIS,FRANCE
关键词
AUTOIMMUNITY; CORTICOID; HYPOPITUITARISM; LYMPHOCYTIC HYPOPHYSITIS; MAGNETIC RESONANCE IMAGING; PITUITARY GLAND;
D O I
10.1227/00006123-199409000-00020
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
WE REPORT THE first case of pseudotumoral lymphocytic hypophysitis successfully treated by corticosteroids without surgery. A 27-year-old woman had been monitored for chronic headache 13 months after giving birth, associated with amenorrhea and galactorrhea. Cranial magnetic resonance imaging revealed a markedly enlarged pituitary gland with a suprasellar extension; the only biochemical abnormality was a mild hyperprolactinemia. Because of a putative diagnosis of prolactinoma, bromocriptine was prescribed at a dose of 5 mg daily, soon followed by the transitory appearance of menstruation. Two years later, panhypopituitarism was present and was revealed by acute adrenal insufficiency. Magnetic resonance imaging revealed that the pituitary mass was the same as previously described, but hormonal investigation showed evidence of complete hypopituitarism and no hyperprolactinemia. Nuclear antibodies were negative as well as other autoantibodies. Human leukocyte antigen serological Class II typing was DR3/DR4. Lymphocytic hypophysitis was then suspected; in the absence of visual complication and because this patient refused surgery, corticosteroids were attempted at a daily dose of 60 mg of prednisone for 3 months, progressively decreased for the next 6 months, Under this treatment, a gradual recovery of all pituitary hormones was observed and magnetic resonance imaging showed a reduction of two-thirds in pituitary mass. Five months after the end of corticoid treatment, our patient relapsed with panhypopituitarism and an increase of pituitary volume. She underwent steroid treatment, and a biopsy was performed and confirmed the diagnosis of autoimmune hypophysitis. Such a case emphasizes the importance of clinical, biological, and radiological criteria leading one to suspect the diagnosis of lymphocytic hypophysitis: steroid treatment proved to be useful in our observation, both in the reduction in tumoral volume and in hormonal recovery.
引用
收藏
页码:505 / 508
页数:4
相关论文
共 19 条
[1]   REVERSIBLE ADRENOCORTICOTROPIN DEFICIENCY DUE TO PROBABLE AUTOIMMUNE HYPOPHYSITIS IN A WOMAN WITH POSTPARTUM THYROIDITIS [J].
BEVAN, JS ;
OTHMAN, S ;
LAZARUS, JH ;
PARKES, AB ;
HALL, R .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1992, 74 (03) :548-552
[2]   THE COURSE OF LYMPHOCYTIC HYPOPHYSITIS [J].
BITTON, RN ;
SLAVIN, M ;
DECKER, RE ;
ZITO, J ;
SCHNEIDER, BS .
SURGICAL NEUROLOGY, 1991, 36 (01) :40-43
[3]  
BORENSZTEIN P, 1989, ANN MED INTERNE, V140, P219
[4]  
Brandes J C, 1989, Wis Med J, V88, P29
[5]   LYMPHOCYTIC HYPOPHYSITIS - REPORT OF 3 NEW CASES AND REVIEW OF THE LITERATURE [J].
COSMAN, F ;
POST, KD ;
HOLUB, DA ;
WARDLAW, SL .
MEDICINE, 1989, 68 (04) :240-256
[6]   LYMPHOCYTIC ADENOHYPOPHYSITIS - A PITUITARY MASS LESION OCCURRING IN PREGNANCY - PROPOSAL FOR MEDICAL-TREATMENT [J].
FEIGENBAUM, SL ;
MARTIN, MC ;
WILSON, CB ;
JAFFE, RB .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1991, 164 (06) :1549-1555
[7]   LYMPHOCYTIC HYPOPHYSITIS IN A MAN [J].
GUAY, AT ;
AGNELLO, V ;
TRONIC, BC ;
GRESHAM, DG ;
FREIDBERG, SR .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1987, 64 (03) :631-634
[8]   LYMPHOCYTIC HYPOPHYSITIS AND PULMONARY SARCOIDOSIS - REPORT OF A CASE [J].
HAYASHI, H ;
YAMADA, K ;
KUROKI, T ;
KATAYAMA, M ;
SHIGEMORI, M ;
KURAMOTO, S ;
NONAKA, K .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1991, 95 (04) :506-511
[9]  
JOSSE RG, 1985, AUTOIMMUNE THYROID D, P405
[10]   LYMPHOCYTIC ADENOHYPOPHYSITIS - CLINICAL, RADIOLOGICAL, AND MAGNETIC-RESONANCE IMAGING CHARACTERIZATION [J].
LEVINE, SN ;
BENZEL, EC ;
FOWLER, MR ;
SHROYER, JV ;
MIRFAKHRAEE, M .
NEUROSURGERY, 1988, 22 (05) :937-941