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Sheehan's syndrome natural history, complications and prognosis

Introduction

Overview

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, and Prognosis

Natural History

Complications

Prognosis

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

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. PMIDΒ 11273296.
  2. ↑ Moreira AC, Zanini Maciel LM, Foss MC, Tabosa VerΓ­ssimo JM, Iazigi N (1984). “Gonadotropin secretory capacity in a patient with Sheehan’s syndrome with successful pregnancies”. Fertil. Steril. 42 (2): 303–5. PMIDΒ 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. PMIDΒ 27359291.

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