| Literature DB >> 20010970 |
Courtney Pendleton1, Hasan A Zaidi, Gustavo Pradilla, Aaron A Cohen-Gadol, Alfredo Quiñones-Hinojosa.
Abstract
BACKGROUND: This case study illustrates Harvey Cushing's pioneering work in pituitary transplantation in the early 20th century and the essential relationship between laboratory research and clinical practice. In 1911, a 48 year-old man presented at Johns Hopkins Hospital with bitemporal hemianopsia, hypothermia, hypersomnolence, decreased libido, polydypsia and polyuria. INVESTIGATION: A review of the Johns Hopkins Hospital surgical records from 1896-1912 on a patient with hypopituitarism secondary to a suprasellar mass, in whom the first documented pituitary gland transplantation was performed. DIAGNOSIS: A diagnosis of hypopituitarism was made. Postmortem examination revealed a cystic cavity lined with squamous epithelium. MANAGEMENT: The patient was treated with whole-gland pituitary extract, which improved his symptoms only temporarily. Cushing transplanted a pituitary gland obtained from a spontaneously aborted fetus into the cerebral cortex of the patient, who showed marked improvement of his somnolence and confusion, whereas his polyuria and polydypsia persisted. A recurrence of symptoms after 6 weeks prompted Cushing to attempt a second transplant of a fetal pituitary gland, without improvement. The patient resumed hormonal supplementation with whole-gland pituitary extract, but died a month after the second transplant from respiratory complications.Entities:
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Year: 2010 PMID: 20010970 DOI: 10.1038/nrendo.2009.223
Source DB: PubMed Journal: Nat Rev Endocrinol ISSN: 1759-5029 Impact factor: 43.330