Sheehan's syndrome , also known as postpartum pituitary gland necrosis , is hypopituitarism decreased functioning of the pituitary gland , caused by ischemic necrosis due to blood loss and hypovolemic shock during and after childbirth. The various signs and symptoms in Sheehan's syndrome are caused by damage to the pituitary, thereby causing a decrease in one or more of the hormones it normally secretes. Because the pituitary controls many glands in the endocrine system , partial or complete loss of a variety of functions may result. Another such feature is secondary adrenal insufficiency lack of ACTH secretion from the anterior pituitary. In a more chronic case, it is similar to Addison's disease with symptoms including fatigue , weight loss , hypoglycemia low blood sugar levels , anemia and hyponatremia low sodium levels.
|Published (Last):||8 May 2013|
|PDF File Size:||12.82 Mb|
|ePub File Size:||18.55 Mb|
|Price:||Free* [*Free Regsitration Required]|
Sheehan's syndrome with central diabetes insipidus. Sheehan's syndrome refers to the occurrence of hypopituitarism after delivery, usually preceded by postpartum hemorrhage. The condition still continues to be a common cause of hypopituitarism in developing countries like India. The disorder usually presents with anterior pituitary failure with preservation of posterior pituitary functions.
Posterior pituitary dysfunction in the form of central diabetes insipidus is rare in patients with Sheehan's syndrome. We describe the clinical course of a young lady who after her sixth childbirth developed severe postpartum hemorrhage followed by development of panhypopituitarism which was confirmed by hormonal investigation and demonstration of empty sella on imaging. In addition, she developed Polyuria. The water deprivation test and response to vasopressin test results indicated central diabetes insipidus.
She needed oral desmopressin on a continuous basis to control polyuria. Keywords: Sheehan's syndrome; central diabetes insipidus; water deprivation test. Sheehan's syndrome SS presents with anterior pituitary hormone deficiency after child birth. Hypopituitarism results as a consequence of infarction and necrosis of the physiologically enlarged pituitary gland during pregnancy which is usually preceded by postpartum hemorrhage.
Pituitary enlargement during pregnancy results in compression of the superior hypophyseal artery. Any hypotension during delivery causes arterial spasm in smaller vessels, apoplexy, and subsequent pituitary necrosis 1. The syndrome manifests with lactation failure, amenorrhea, involution of the breasts, and loss of axillary and pubic hair and of features typical of other anterior pituitary hormone deficiencies 2. Pathogenesis of SS is not clear. A role of autoimmunity in the development of hypopituitarism has been suggested.
It is believed that tissue necrosis may release sequestered antigens, triggering pituitary autoimmunity and delayed hypopituitarism 3.
Most patients present with either complete or partial hypofunction of the anterior pituitary Although subtle posterior pituitary disturbances in these patients have been reported, complete central diabetes insipidus CDI is rare and most cases are reported before the availability of magnetic resonance imaging We report the clinical course of a case of Sheehan's syndrome who also presented with severe polyuria during follow-up and on investigation was found to have CDI which responded to oral desmopressin.
A year-old woman delivered her sixth child, developed massive postpartum bleeding, and received three units of blood after hospitalization three years before seeking us. After delivery she failed to lactate, did not menstruate and was fatigable. A year earlier, she had also started noticing excessive thirst and polyuria. Investigation revealed anemia Hb of 9.
Biochemical investigation revealed normal glucose, sodium, potassium, urea, creatinine, and calcium levels. Her chest X-ray and electrocardiogram were within normal limits. Basal hormone estimations revealed undetectable serum total thyroxine T4 , inappropriately normal thyroid stimulating hormone TSH with low basal cortisol, growth hormone GH , prolactin PRL , and gonadotrophins; features suggestive of panhypopituitarism Table 1.
Magnetic resonance imaging MRI of the pituitary revealed evidence of completely empty sella Figure 1. Some of her symptoms started improving over the following two weeks but polyuria worsened, urinary volume increased from 4.
The patient was discharged and was readmitted after two months for evaluation of polyuria and water deprivation test was planned. The procedure of the water deprivation test was explained to the patient and her spouse and informed consent was obtained from both of them.
The patient was subjected to the Miller procedure water deprivation test She was deprived of food and water from 9 p. Her weight, blood pressure, urine volume, urinary osmolality, plasma sodium, and glucose were measured at 7 o'clock in the morning; her weight, blood pressure, urine volume, and urine osmolality were measured hourly until urinary osmolality stabilized.
At this time, plasma sodium and osmolality were measured and 5 units of arginine vasopressin AVP were administered subcutaneously. Subsequently, urine and plasma osmolality were measured every thirty minutes for next 90 minutes. The patient's husband was also submitted to the tests in the same manner and acted as a control. All osmolality studies were performed with an osmometer using the freezing point depression method. The patient was put on oral desmopressin 0.
The present patient had classical presentation of Sheehan's syndrome evidenced by history of postpartum hemorrhage followed by lactation failure, amenorrhea, and features of hypothyroidism. Hormonal analysis revealed evidence of panhypopituitarism and MRI revealed features of empty sella. She had a history of polyuria for one year before admission and there was an exacerbation after achieving euthyroid and eucortisolemic states.
The water deprivation test documented diabetes insipidus and response to AVP confirmed central diabetes insipidus. Although SS clinically comes to medical attention with features of anterior pituitary hormone deficiency, interest in the posterior pituitary function has been there since the original description of the disease, when Sheehan noticed atrophic changes in the posterior pituitary Posterior pituitary functions have been tested in many series of patients with SS and subtle defects in AVP secretion have been detected In one of the recently published series around 29 percent of the patients had partial central diabetes insipidus and the threshold for thirst was increased in all of them Polyuria of the magnitude needing treatment on a permanent basis is rare in patients with SS and data is limited to case reports only.
The fact that involvement of the posterior pituitary is less common than that of the anterior pituitary is partly explained by the difference in vascular supply in the two regions. The inferior hypophysial arteries arising from the cavernous portion of the internal carotid artery divide into medial and lateral arteries. These arteries join with those from the opposite side forming an anastomotic ring around the infundibular process of the neurohypophysis and protect it from excessive damage In one of our large clinical studies previously published; two out of the eighty six patients of SS who had adverse post delivery outcome had Central DI.
Both needed nasal desmopressin for control of polyuria and died after six weeks, 5. Tulandi and cols. She developed polyuria seven months later and was diagnosed to have diabetes insipidus , imaging of the brain revealed empty sella.
Weston and cols. Postoperatively, she developed excessive thirst, polyuria, severe headaches, and blurry vision. Pituitary function tests revealed central hypothyroidism, hypoprolactinemia, and secondary adrenal failure.
Diabetes insipidus was confirmed with electrolyte testing before and after a hour water deprivation test. Imaging showed evidence of ischemic infarction of the pituitary gland. Kan and cols. She had an estimated blood loss of mL, her hemoglobin dropped from 9. Investigations confirmed central DI and cerebral computed tomography revealed normal pituitary.
She required treatment with desmopressin for a few days only. It is possible that the said patient had DI before delivery and was compensating by taking more water and became symptomatic only after water was restricted during the cesarean section or else DI was transient.
Recently Kumar and cols. Patients with SS have elevated AVP levels and increased sensitivity to the hormone before treatment, mainly contributed by a hypocortisol state. If present, ADH deficiency usually comes to attention after institution of steroid treatment when the subtle deficiency becomes symptomatic 17, Although the present patient had Polyuria for one year, she became more symptomatic after replacement of prednisolone and thyroxine and required permanent treatment after documentation of central diabetes insipidus.
In summary a young woman developed postpartum hemorrhage, needed blood transfusion after delivery of her 6 th child, and subsequently developed Sheehan's syndrome confirmed by hormonal investigation and imaging.
She also developed polyuria and was confirmed to have central diabetes insipidus by a water deprivation test. She needed oral desmopressin permanently to be free of polyuria. Permanent central diabetes insipidus in patients with Sheehan's syndrome is rare. Disclosure: no potential conflict of interest relevant to this article was reported. Sheehan's syndrome: differential diagnosis in acute phase. J Intern Med. Pituitary autoimmunity in patients with Sheehan's syndrome.
J Clin Endocrinol Metab. Sheehan HL. The incidence of postpartum hypopituitarism. Am J Obstet Gynecol. Kelestimur F. Sheehan's syndrome. Clinical spectrum of Sheehan's syndrome. Ann Saudi Med. Multiple spontaneous pregnancies in Sheehan's syndrome with preserved gonadotroph function.
Bakiri F, Benmiloud M. Antidiuretic function in Sheehan's syndrome. Br Med J. An assessment of posterior pituitary function in patients with Sheehan's syndrome. Clin Endocrinol Oxf. Kan AK, Calligerous D. A case report of Sheehan syndrome presenting with diabetes insipidus. Recognition of partial defects in antidiuretic hormone secretion. Ann Intern Med. Sheehan HL, Whitehead R. The neurohypophysis in postpartum hypopituitarism. J Pathol Bacteriol. Posterior pituitary function in Sheehan's syndrome.
2014, Número 04
Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed. Sheehan syndrome is a rare, acquired, pituitary hormone deficiency disorder resulting from pituitary necrosis following peri- or postpartum hemorrhage characterized by various symptoms depending on resulting hormone decrease e.
It only occurs in postpartum females who experience large volume hemorrhage and hypovolemic shock, either during delivery or afterward with resultant necrosis of anterior pituitary cells 4. Advances in obstetrical care mean Sheehan syndrome is rare in developed countries. Incidence in developing and low-income countries is as high as 5 per births 5. Hyperplasia of pituitary cells, particularly lactotrophs, occurs in the weeks preceding delivery resulting in an increased metabolic demand without a concomitant increase in blood supply 4.
NCBI Bookshelf. Mark P. Schury ; Rotimi Adigun. Authors Mark P. Schury 1 ; Rotimi Adigun 2.