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Table 2 A summary of the literature review findings for acute Sheehan syndrome

From: A case of acute Sheehan’s syndrome and literature review: a rare but life-threatening complication of postpartum hemorrhage

First author

Year (Reference number)

Age (years)

Day

cause of hemorrhage

 

Blood loss

Hb level

Shock

DIC

Symptom

Headache

Etiology

Treatment

Putterman C

1991 [9]

27

7 days

uterine atony

vaginal delivery

estimated blood loss was 2 L

not described

presented

not described

paresthesia

not described

hyponatremia, adrenal insufficiency

hydrocortisone, levothyroxine, estrogen and progesterone

The patient was resuscitated with blood and colloids; hemorrhage was controlled with uterine massage, oxytocin, and ergotamine.

Syndrome of inappropriate secretion of antidiuretic hormone caused by Sheehan’s syndrome should be considered in the differential diagnosis of postpartum hyponatremia.

Zuker N

1995 [10]

20

14 h

uterine atony

vaginal delivery

1200 mL

Decreased to 5.1 g/dl

presented

presented

hypoglycemia

not described

adrenal insufficiency

hydrocortisone.

An urgent subtotal hysterectomy was performed due to life threatening hemorrhage.

Acute hypoglycemic coma as the initial manifestation of Sheehan’s syndrome in the first few hours postpartum is extremely rare.

Lavallee G

1995 [11]

30

6 h

uterine inversion

vaginal delivery

not described

Decreased to 7.6 g/dl

not presented

not described

generalized tonic-clonic convulsions

presented

adrenal insufficiency

hydrocortisone and levothyroxine

She underwent a uterine revision under 5 mg intravenous midazolam hydrochloride.

MR was performed 6 days after delivery; a large intrasellar mass with superior extension was confirmed on T1-weighted. The mass effect has disappeared, and the pituitary gland is somewhat atrophic (postpartum day 48)

It is therefore important to be alert to the possibility that an enlarged nonhemorrhagic pituitary gland may be present in the post-infarction phase of Sheehan’s syndrome, as shown in the present case report

Kan AK

1998 [12]

32

24 h

unclear

cesarean section

500 mL

Decreased to 5.7 g/dl

not presented

not described

excessive urination

not described

diabetes insipidus

desmopressin

She was transfused 4 units of blood and additional treatment was not performed.

This is a report of a case of diabetes insipidus developing within 24 h postpartum in a grand multipara who had an elective lower segment Cesarean section for twins.

Dejager S

1998 [13]

32

3 days

*

not described

little

not described

presented

not described

Severe headache excessive urination

presented

diabetes insipidus

hydrocortisone and desmopressin

The delivery was complicated by a occurrence of a severe hypotention episode at the beginning of the epidural anesthesia.

MRI was performed 6 days after delivery. MRI revealed the presence of a holosellar 11-mm diameter mass.

Follow-up MRI showed a spontaneous and rapid shrinkage of the pituitary, within 20 days, which appeared as an empty sella 3 months later.

Sheehan’s syndrome may initially closely mimic hypophysitis, or the necrosis of an adenoma.

Boulanger E

1999 [14]

30

10 days

uterine scar disjunction

VBAC

not described

not described

not described

presented

asthenia

not described

hyponatremia, adrenal insufficiency

glucocorticoids.

Hysterectomy was performed to control blood loss and transient disseminated intravascular coagulation occurred.

MRI was not performed.

The report of early and acute hyponatremia with inappropriate secretion of antidiuretic hormone occurring 10 days after vaginal delivery with severe blood loss.

Kale K

1999 [15]

23

20 days

not described

not described

not described

not described

not described

not described

psychosis

not described

maybe hypothyroidism

predonisolone and thyroxine sodium

The treatment to control the bleeding was not described.

        

MRI was not performed.

            

It was interesting to note that all the clinical features of Sheehan’s syndrome and psychosis improved with hormone replacement therapy and she did not require treatment with antipsychotic medications.

  

Schrager S

2001 [16]

39

12 days

atonic bleeding

cesarean delivery

severe

not described

presented

feeling nausea

general fatigue

not described

hyponatremia, adrenal insufficiency

cortisone acetate

Hysterectomy was performed to control blood loss and underwent an embolization of her right vaginal artery.

A sodium level measured on the 5th day of her hospitalization was normal.

Although Sheehan’s syndrome is uncommon as a result of improved obstetric care, it should be a consideration in any woman who has a history of a postpartum hemorrhage and who reports signs or symptoms of pituitary deficiency.

Lust K

2001 [17]

32

3 days

atonic bleeding

vaginal delivery

3200 ml

not described

presented

presented

headache

presented

hyponatremia

thyroxine and cortisone acetate

Uterotonic agents successfully controled the bleeding.

MRI scan of pituitary day five after delivery showed the enlarged pituitary gland with its superior margin reaching the undersurface of the optic chiasm.

MRI scan of pituitary 4 months after delivery showed atrophic pituitary gland and empty sella.

Wang HY

2002 [18]

32

7 days

persistent bleeding from uterus

cesarean delivery

severe

3.5 g/dL

presented

presented

excessive urination

not described

diabetes insipidus

desmopressin

Angiography with bilateral uterine artery embolization was performed.

MRI was not performed.

There are very few existing literature discussing concomitant Sheehan’s syndrome and acute renal failure.

Bunch TJ

2002 [19]

23

6 days

atonic bleeding

cesarean delivery

massive hemorrhage

not described

presented

presented

general fatigue

not described

hyponatremia, adrenal insufficiency

predonisolone and levothyroxine

She received large volumes of fluid and blood products for resuscitation. Additional treatment was not performed.

MRI demonstrates an enlarged pituitary gland with abnormal signal on the T1 weighted precontrast images (postpartum approximately day 10).

There are many studies describing complications of late Sheehan’s syndrome; however, relatively few contain descriptions of the acute phase.

Munz W

2004 [20]

33

6 days

  

Hb level decreased to 3.0 g/dL

   

headache, vomitting

 

hyponatremia, adrenal insufficiency

hydrocortisone and levothyroxine

Hysterectomy was performed to control blood loss. The patient received a transfusion of 12 units of blood and six units of fresh frozen plasma.

MRI of the pituitary was normal on postpartum day 6.

Sheehan’s syndrome can be associated with hyponatremia, illustrating the need to include hyponatremia as an initial symptom in the differential diagnosis of Sheehan’s syndrome.

Wang S

2005 [21]

33

19 days

postpartum hemorrhage

cesarean delivery

Massive bleeding

6.6 g/dL

presented

presented

hemodynamic instability

not described

adrenal insufficiency

hydrocortisone and thyroxine sodium

Hysterectomy was performed to control blood loss.

MRI showed no notable abnormality (postpartum day 19).

MRI showed a flattened pituitary gland and loculation of cerebrospinal fluid (postpartum day 32).

Although the occurrence of Sheehan’s syndrome is now rare, it should still be considered in any woman with a history of peripartum hemorrhage who develops manifestations of pituitary hormone deficiency.

Kaplun J

2008 [22]

29

17 days

retained placenta

unknown

massive

3.8 g/dL

not described

not described

general fatigue

presented

panhypopituitarism

not described

  

21

3 days

perineal laceration

vaginal delivery

massive

5.5 g/dL

presented

not described

fever and a severe headache

not presented

hyponatremia, adrenal insufficiency

prednisone and levothyroxine

The treatment used to control the bleeding was not described for either case 1 or 2.

MRI on postpartum day 26 revealed a nonenhancing, minimally hypointense lesion in the pituitary gland (case 1).

MRI obtained on postpartum day 6 showed an enlarged pituitary gland with suprasellar extension to the optic chiasm (case 2).

Anfuso S

2009 [23]

35

8 days

none

vaginal delivery

500 mL

8.8 g/dL

not presented

not presented

asthenia, persistent headache

not presented

hyponatremia, adrenal insufficiency

hydrocortisone and levothyroxine

The treatment to control the bleeding was not described.

MRI on postpartum day 8 revealed an abnormal lack of enhancement of pituitary grand.

MRI 3 months postpartum confirmed previous vascular necrosis.

Early diagnosis of early-onset Sheehan’s syndrome associated with severe hyponatremia, following dystocic childbirth complicated by postpartum hemorrhage.

Kumar S

2011 [24]

36

4 days

atonic bleeding

vaginal delivery

massive

6.1 g/dL

presented

presented

excessive urination

not presented

diabetes insipidus

desmopressin

Hysterectomy was performed to control the blood loss. The patient received the massive transfusion.

MRI showed a normal pituitary gland (postpartum day 6).

It is important to consider posterior pituitary ischemia resulting from Sheehan’s syndrome, presenting as central diabetes insipidus, as a cause of polyuria. Appropriate hormonal replacement that is initiated early can improve the clinical status and outcomes of patients.

Shoib S

2013 [25]

31

16–18 days

unknown

unknown

not described

not described

not described

not described

psychosis

not described

possibly hypothyroidism

prednisolone and thyroxine sodium

The treatment to control the bleeding was not described.

CT and MRI scans were not performed.

Psychosis in patients with Sheehan’s syndrome is uncommon. Clinicians should have a high index of suspicion when postpartum-psychosis presents with a significant obstetric history.

Sasaki S

2014 [26]

37

4–6 days

retained placenta

vaginal delivery

massive

4.0 g/dL

presented

presented

failure to lactate

not described

panhypopituitarism

hydrocortisone.

Emergency uterine embolization was performed.

Sagittal T1-weighted image showing slight swelling of the anterior lobe and the pituitary stalk (postpartum day 10).

At 1 month after delivery, swelling of the anterior lobe was reversed.

At 5 months after delivery, marked atrophy of the anterior lobe was observed

Hale B

2014 [27]

31

6 days

retained placenta

vaginal delivery

1500 ml

6.2 g/dL

presented

presented

headache, failure to lactate, fatigue

presented

partial hypopituitarism

prednisone, levothyroxine, desmopressin and somatropin

Retained placenta required manual extraction.

Cranial magnetic resonance imaging scan performed on postpartum day six. The pituitary gland appears enlarged with peripheral enhancement and an isodense central area.

Postpartum headache is a common occurrence with a broad differential diagnosis. Combined pathophysiological features of Sheehan’s syndrome and postpartum headache is an atypical acute presentation.

Present case

2015

27

8 days

atonic bleeding

vaginal delivery

at least 5000 mL

4.1 g/dl

presented

presented

grand mal convulsion

not presented

hyponatremia, adrenal insufficiency

hydrocortisone and thyroxine sodium

Emergency uterine embolization was performed to control the blood loss.

A sagittal T1-weighted image of the pituitary gland was normal on postpartum day 15.

At 6 months after delivery, marked atrophy of the anterior lobe was observed.

Early onset of Sheehan’s syndrome is rare. Acute Sheehan’s syndrome presenting with a sudden onset of postpartum seizures is rarer still.

VBAC: Vaginal birth after cesarean section

  1. *Severe hypotension episode at the beginning of the epidural anesthesia with loss of consciousness was observed
  2. Abbreviations: CT computed tomography, Hb hemoglobin, MRI magnetic resonance imaging