Autoimmune polyglandular syndrome, primary empty sella, and acute lymphocytic leukaemia.

Abstract:

:A young man is reported with an autoimmune polyglandular syndrome (APS) characterized by Addison's disease, primary hypothyroidism, primary hypogonadism, vitiligo, associated with primary empty sella and partial impairment of pituitary hormone secretion. Two years later the patient showed a null cell type acute lymphocytic leukaemia, immediately after surgery for an inguinal hernia. Pathogenetic mechanisms are postulated on the basis of HLA studies and lymphocytic typing.

journal_name

Clin Endocrinol (Oxf)

journal_title

Clinical endocrinology

authors

De Rosa G,Della Casa S,Corsello SM,Cecchini L,Callà C

doi

10.1111/j.1365-2265.1987.tb01183.x

subject

Has Abstract

pub_date

1987-11-01 00:00:00

pages

535-43

issue

5

eissn

0300-0664

issn

1365-2265

journal_volume

27

pub_type

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