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Sheehan's syndrome natural history, complications and prognosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Iqra Qamar M.D.[2]

Overview

Sheehan’s syndrome leads to hypopituitarism and empty sella syndrome, if left untreated. Common complications are including adrenal crisis, hypotension, hypothyroidism, and hypopituitarism. Prognosis is generally excellent provided early diagnosis and management resulting in complete reversal of symptoms.

Natural History, Complications, and Prognosis

Natural History

Complications

Prognosis

  • Prognosis is generally good, and results in reversal of symptoms once respective hormones are being replaced.

References

  1. Zargar AH, Masoodi SR, Laway BA, Sofi FA, Wani AI (1998). “Pregnancy in Sheehan’s syndrome: a report of three cases”. J Assoc Physicians India. 46 (5): 476–8. PMID 11273296.
  2. Moreira AC, Zanini Maciel LM, Foss MC, Tabosa Veríssimo JM, Iazigi N (1984). “Gonadotropin secretory capacity in a patient with Sheehan’s syndrome with successful pregnancies”. Fertil. Steril. 42 (2): 303–5. PMID 6745465.
  3. Laway BA, Ramzan M, Allai MS, Wani AI, Misgar RA (2016). “CARDIAC STRUCTURAL AND FUNCTIONAL ABNORMALITIES IN FEMALES WITH UNTREATED HYPOPITUITARISM DUE TO SHEEHAN SYNDROME: RESPONSE TO HORMONE REPLACEMENT THERAPY”. Endocr Pract. 22 (9): 1096–103. doi:10.4158/EP161262.OR. PMID 27359291.

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