Sheehan's syndrome differential diagnosis: Difference between revisions

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|oligo/amenorrhea
|Oligo/amenorrhea
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* Adrenal insufficiency symptoms
* Adrenal insufficiency symptoms


* Hypothyroidism features
* Hypothyroidism features
|<nowiki>-Breast tissue atrophy</nowiki>
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* Breast tissue atrophy


-decreased axillary and pubic hair growth
* Decreased axillary and pubic hair growth
|Pancytopenia
|Pancytopenia


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|<nowiki>+/-</nowiki>
|<nowiki>++</nowiki>
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|oligo/amenoorhea
|Oligo/amenorrhea
|Severe [[headache]]
|Severe [[headache]]
* [[Nausea and vomiting]]
* [[Nausea and vomiting]]
* Paralysis of eye muscles ([[diplopia]])
* Paralysis of eye muscles ([[diplopia]])
* Changes in vision
* Changes in vision
|<nowiki>-Visual acuity defects</nowiki>
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* Visual acuity defects


-CN palsies (nerves III, IV, V, and VI)
* CN palsies (nerves III, IV, V , and VI)


|Decreased levels of anterior pituitary hormones in blood.
|Decreased levels of anterior pituitary hormones in blood.
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|oligo/amenoorhea
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|<nowiki>-Associated with autoimmune conditions</nowiki>
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* Associated with autoimmune conditions
 
* Generalized [[headache]]
* Generalized [[headache]]


* Retro-orbital or Bitemporal [[pain]]
* Retro-orbital or Bitemporal [[pain]]
* Most often seen in late [[pregnancy]] or the [[postpartum]] period


* Mass lesion effect such as [[Visual field defect|visual field defects]]
* Mass lesion effect such as [[Visual field defect|visual field defects]]
* [[Hypopituitarism]]
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|<nowiki>-DI</nowiki>
* DI


-Autoimmune thyroiditis
* Autoimmune thyroiditis
|<nowiki>-Decreased pituitary hormones(Gonadotropins most common)</nowiki>
|<nowiki>-Decreased pituitary hormones(Gonadotropins most common)</nowiki>


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* [[Headache|Severe headache]]
* [[Thunderclap headache|Thunderclap]] [[Headache|headache]]( worst [[headache]] of life)
* [[Thunderclap headache|Thunderclap]]
* Described as the worst [[headache]] of life


* [[Double vision]]
* [[Double vision]]
* [[Nausea]] and [[vomiting]]
* [[Nausea]] and [[vomiting]]
* Symptoms of [[meningeal irritation]]
* Symptoms of [[meningeal irritation]]
* Sudden [[Loss of consciousness|decreased level of consciousness]]
|<nowiki>-Signs of meningeal irritation</nowiki>
|<nowiki>-Signs of meningeal irritation</nowiki>


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|<nowiki>-Erectile dysfunction</nowiki>
|<nowiki>-Erectile dysfunction</nowiki>


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|oligo/aenorrhea
|Oligo/amenorrhea
|<nowiki>-Cachexia</nowiki>
|<nowiki>-Cachexia</nowiki>


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or menorrhagia
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|Hot flushes
|Hot flushes


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Revision as of 20:01, 22 August 2017

Sheehan's syndrome Microchapters

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Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Sheehan's syndrome from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Criteria

History and Symptoms

Physical Examination

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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 syndrome must be differentiated from lymphocytic hypophysitis, pituitary apoplexy, hypothyroidism, Addison's disease, panhypopititarism, empty sella syndrome, hypogonadotropic hypogonadism, Simmond's disease, hypoprolactinemia, menopause,female athlete triadand SAH.[1][2][3]

Differentiating Sheehan's Syndrome from other Diseases

Sheehan's syndrome should be differentiated from other diseases causing hypopituitarism.[4][5][6][7][8][9]

Diseases Onset Manifestations Diagnosis
History and Symptoms Physical examination Laboratory findings Gold standard Imaging Other investigation findings
Trumatic delivery Lactation failure Menstrual irregularities Other features
Sheehan's syndrome Acute ++ ++ Oligo/amenorrhea
  • Adrenal insufficiency symptoms
  • Hypothyroidism features
  • Breast tissue atrophy
  • Decreased axillary and pubic hair growth
Pancytopenia

Eosinophilia

Hyponatremia

Low fasting plasma glucose

Decreased levels of anterior pituitary hormones in blood.

Dx is clinical with key feature of traumatic delivery.

-Most senitive test is low baseline prolactin levels w/o response to TRH.

Sequential changes of pituitary enlargement followed by shrinkage and necrosis leading to decreased sellar volume or empty sella.
Pituitary apoplexy Acute +/- ++ Oligo/amenorrhea Severe headache
  • Visual acuity defects
  • CN palsies (nerves III, IV, V , and VI)
Decreased levels of anterior pituitary hormones in blood. MRI
  • MRI is done in cases of inconclusive CT. An MRI is more sensitive in identifying intrasellarmass and soft tissue changes

Blood tests may be done to check:

Lymphocytic hypophysitis Acute +/- + Oligo/amenorrhea
  • Associated with autoimmune conditions
  • Retro-orbital or Bitemporal pain
  • DI
  • Autoimmune thyroiditis
-Decreased pituitary hormones(Gonadotropins most common)

-Hyperprolactinemia

-GH excess

Pituitary biopsy CT & MRI typically reveal --features of a pituitary mass

-diffuse and homogeneous contrast enhancement

The most accurate test is a pituitarybiopsy which will show lymphocyticinfiltration.
Subarachnoid hemorrhage Acute - - - -Signs of meningeal irritation Xanthochromia Digital subtraction angiography

Lumbar puncture (LP) is necessary when there is a strong suspicion of subarachnoid hemorrhage. LP will show:

Empty sella syndrome Chronic - + Oligo/amenorrhea -Erectile dysfunction

-Headache

-Low libido

-Nipple discharge

Signs of raised intracranial pressure may be present Decreased levels of pituitary hormones in blood. MRI Empty sella containing CSF
Simmond's disease/Pituitary chachexia Chronic +/- + Oligo/amenorrhea -Cachexia

-Premature aging

-Progressive emaciation

-Loss of body hair

Decreased levels of anterior pituitary hormones in blood.
Primary hypothyroidism Chronic +/- - Oligomenorrhea menorrhagia
  • Cold intolerance
  • Constipation
Dry skin

Bradycardia

Hair loss

Myxedema

Delayed relaxation phase of deep tendon reflexe

low T3,T4

High TSH

Rest of pituitary hormone levels WNL

TSH levels Done to rule out ant pituitary cause
Primary hypogonadotropic hypogonadism Chronic - - Hot flushes

Energy and mood changes

Decreased libido

Low estrogen, testosterone

High FSH/LH

  • Done to rule out any pituitary cause
  • Blood tests for anemia and iron
  • Genetic tests including a karyotype to check chromosomal structure
  • Prolactin level (milk hormone)
  • Sperm count
  • Thyroid tests
Hypoprolactinemia Chronic - + - Infertility

Subfertiliy

Puerperal agalactogenesis No workup is necessary Done to rule out any pituitary cause -Prolactin assay in 3rd trimester

-LH, FSH

-Thyrotropin and free thyroxine

Panhypopituitarism Chronic - + oligo/amenorrhea Polyuria

Polydipsia

-Growth failure

-B/L hemianopsia

-Papilledema

all pituitary hormones decreased MRI Left hand and wrist radiograph for bone age
Primary adrenal insufficiency/Addison's disease Chronic - - - Hypoglycemia

Hypotension

-Dehydration

-Hyperpigmentation

-loss of pubic and axillary hair

-Hyponatremia with/without hyperkalemia

-Plasma renin activity to aldosterone ratio

CT abdomen CT abdomen -Serum cortisol testing

-Serum ACTH testing

-Antiadrenal Ab testing

Menopause Chronic oligo/amenorrhea
Female athlete triad Chronic oligo/amenorrhea
  1. Rolih CA, Ober KP (1993). "Pituitary apoplexy". Endocrinol. Metab. Clin. North Am. 22 (2): 291–302. PMID 8325288.
  2. Vidal E, Cevallos R, Vidal J, Ravon R, Moreau JJ, Rogues AM, Loustaud V, Liozon F (1992). "Twelve cases of pituitary apoplexy". Arch. Intern. Med. 152 (9): 1893–9. PMID 1520058.
  3. Lazaro CM, Guo WY, Sami M, Hindmarsh T, Ericson K, Hulting AL, Wersäll J (1994). "Haemorrhagic pituitary tumours". Neuroradiology. 36 (2): 111–4. PMID 8183446.
  4. Sato N, Sze G, Endo K (1998). "Hypophysitis: endocrinologic and dynamic MR findings". AJNR Am J Neuroradiol. 19 (3): 439–44. PMID 9541295.
  5. Powrie JK, Powell M, Ayers AB, Lowy C, Sönksen PH (1995). "Lymphocytic adenohypophysitis: magnetic resonance imaging features of two new cases and a review of the literature". Clin. Endocrinol. (Oxf). 42 (3): 315–22. PMID 7758238.
  6. Honegger J, Schlaffer S, Menzel C, Droste M, Werner S, Elbelt U, Strasburger C, Störmann S, Küppers A, Streetz-van der Werf C, Deutschbein T, Stieg M, Rotermund R, Milian M, Petersenn S (2015). "Diagnosis of Primary Hypophysitis in Germany". J. Clin. Endocrinol. Metab. 100 (10): 3841–9. doi:10.1210/jc.2015-2152. PMID 26262437.
  7. Thodou E, Asa SL, Kontogeorgos G, Kovacs K, Horvath E, Ezzat S (1995). "Clinical case seminar: lymphocytic hypophysitis: clinicopathological findings". J. Clin. Endocrinol. Metab. 80 (8): 2302–11. doi:10.1210/jcem.80.8.7629223. PMID 7629223.
  8. Imura H, Nakao K, Shimatsu A, Ogawa Y, Sando T, Fujisawa I, Yamabe H (1993). "Lymphocytic infundibuloneurohypophysitis as a cause of central diabetes insipidus". N. Engl. J. Med. 329 (10): 683–9. doi:10.1056/NEJM199309023291002. PMID 8345854.
  9. Hsieh CY, Liu BY, Yang YN, Yin WH, Young MS (2011). "Massive pericardial effusion with diastolic right ventricular compression secondary to hypothyroidism in a 73-year-old woman". Emerg Med Australas. 23 (3): 372–5. doi:10.1111/j.1742-6723.2011.01425.x. PMID 21668725.

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