Sheehan's syndrome natural history, complications and prognosis: Difference between revisions

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{{Sheehan's syndrome}}
{{Sheehan's syndrome}}
{{CMG}}; {{AE}}  
{{CMG}}; {{AE}}{{IQ}}  


==Overview==
==Overview==
*Sheehan syndrome, if left untreated lead to mitral regurgitation, pericardial effusion and diminished LVM.<ref name="pmid27359291">{{cite journal |vauthors=Laway BA, Ramzan M, Allai MS, Wani AI, Misgar RA |title=CARDIAC STRUCTURAL AND FUNCTIONAL ABNORMALITIES IN FEMALES WITH UNTREATED HYPOPITUITARISM DUE TO SHEEHAN SYNDROME: RESPONSE TO HORMONE REPLACEMENT THERAPY |journal=Endocr Pract |volume=22 |issue=9 |pages=1096–103 |year=2016 |pmid=27359291 |doi=10.4158/EP161262.OR |url=}}</ref>
[[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.
*Common complications of [disease name] include [complication 1], [complication 2], and [complication 3].
*Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately [#]%.


==Natural History, Complications, and Prognosis==
==Natural History, Complications, and Prognosis==


===Natural History===
===Natural History===
*The symptoms of (disease name) usually develop in the first/ second/ third decade of life, and start with symptoms such as ___.  
*Sheehan's syndrom<nowiki/>e usually results in [[anterior pituitary]] shrinkage within 20 days, followed by disappearance of pituitary tissue in 6-8 week; resulting in [[hypopituitarism]] and [[empty sella syndrome]].
*The symptoms of (disease name) typically develop ___ years after exposure to ___.  
*The symptoms of [[Sheehan's syndrome]] can develop during immediate post-puerperal period to years after delivery.
*If left untreated, [#]% of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
*It may result in sparing or reversal of gonadotropic dysfunction as few cases of successful pregnancies have been reported following Sheehan's syndrome.<ref name="pmid11273296">{{cite journal |vauthors=Zargar AH, Masoodi SR, Laway BA, Sofi FA, Wani AI |title=Pregnancy in Sheehan's syndrome: a report of three cases |journal=J Assoc Physicians India |volume=46 |issue=5 |pages=476–8 |year=1998 |pmid=11273296 |doi= |url=}}</ref><ref name="pmid6745465">{{cite journal |vauthors=Moreira AC, Zanini Maciel LM, Foss MC, Tabosa Veríssimo JM, Iazigi N |title=Gonadotropin secretory capacity in a patient with Sheehan's syndrome with successful pregnancies |journal=Fertil. Steril. |volume=42 |issue=2 |pages=303–5 |year=1984 |pmid=6745465 |doi= |url=}}</ref>
*If left untreated, lead to [[mitral regurgitation]], [[pericardial effusion]], and diminished left ventricular motion, [[Adrenal crisis|adrenal crisi]]<nowiki/>s, [[hypopituitarism]], and [[empty sella syndrome]].<ref name="pmid27359291">{{cite journal |vauthors=Laway BA, Ramzan M, Allai MS, Wani AI, Misgar RA |title=CARDIAC STRUCTURAL AND FUNCTIONAL ABNORMALITIES IN FEMALES WITH UNTREATED HYPOPITUITARISM DUE TO SHEEHAN SYNDROME: RESPONSE TO HORMONE REPLACEMENT THERAPY |journal=Endocr Pract |volume=22 |issue=9 |pages=1096–103 |year=2016 |pmid=27359291 |doi=10.4158/EP161262.OR |url=}}</ref>


===Complications===
===Complications===
*Common complications of [disease name] include:
*Common complications of Sheehan's syndrome are including:
**[complication 1]
**[[Adrenal crisis]]
**[complication 2]
**[[Hypotension]]
**[complication 3]
**[[Hypothyroidism]]
**[[Menstrual irregularities]]
**[[Empty sella syndrome]]


===Prognosis===
===Prognosis===
*Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately [#]%.
*[[Prognosis]] is generally good, and results in reversal of symptoms once respective [[hormones]] are being replaced.
*Depending on the extent of the [tumor/disease progression/etc.] at the time of diagnosis, the prognosis may vary. However, the prognosis is generally regarded as poor/good/excellent.
*The presence of [characteristic of disease] is associated with a particularly [good/poor] prognosis among patients with [disease/malignancy].
*[Subtype of disease/malignancy] is associated with the most favorable prognosis.
*The prognosis varies with the [characteristic] of tumor; [subtype of disease/malignancy] have the most favorable prognosis.


==References==
==References==
{{Reflist|2}}
{{Reflist|2}}
 
{{WH}}
{{WH}}
{{WS}}
{{WS}}
[[Category:Medicine]]
[[Category:Endocrinology]]
[[Category:Up-To-Date]]
[[Category:Emergency medicine]]
[[Category:Obstetrics]]

Latest revision as of 00:09, 30 July 2020

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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]

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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