Sheehan syndrome

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Sheehan syndrome

Metabolism HYMS year 3

Metabolism HYMS year 3

Anatomy of the abdominal viscera: Kidneys, ureters and suprarenal glands
Anatomy of the urinary organs of the pelvis
Anatomy of the female urogenital triangle
Anatomy of the perineum
Anatomy clinical correlates: Male pelvis and perineum
Anatomy clinical correlates: Female pelvis and perineum
Development of the renal system
Ureter, bladder and urethra histology
Kidney histology
Renal system anatomy and physiology
Hydration
Body fluid compartments
Movement of water between body compartments
Renal clearance
Glomerular filtration
TF/Px ratio and TF/Pinulin
Measuring renal plasma flow and renal blood flow
Regulation of renal blood flow
Tubular reabsorption and secretion
Tubular secretion of PAH
Tubular reabsorption of glucose
Urea recycling
Tubular reabsorption and secretion of weak acids and bases
Proximal convoluted tubule
Loop of Henle
Distal convoluted tubule
Renin-angiotensin-aldosterone system
Sodium homeostasis
Potassium homeostasis
Phosphate, calcium and magnesium homeostasis
Osmoregulation
Antidiuretic hormone
Kidney countercurrent multiplication
Free water clearance
Vitamin D
Erythropoietin
Physiologic pH and buffers
Buffering and Henderson-Hasselbalch equation
The role of the kidney in acid-base balance
Acid-base map and compensatory mechanisms
Respiratory acidosis
Metabolic acidosis
Plasma anion gap
Respiratory alkalosis
Metabolic alkalosis
Renal agenesis
Horseshoe kidney
Potter sequence
Hyperphosphatemia
Hypophosphatemia
Hypernatremia
Hyponatremia
Hypermagnesemia
Hypomagnesemia
Hyperkalemia
Hypokalemia
Hypercalcemia
Hypocalcemia
Renal tubular acidosis
Minimal change disease
Diabetic nephropathy
Focal segmental glomerulosclerosis (NORD)
Amyloidosis
Membranous nephropathy
Lupus nephritis
Poststreptococcal glomerulonephritis
Rapidly progressive glomerulonephritis
IgA nephropathy (NORD)
Alport syndrome
Kidney stones
Hydronephrosis
Acute pyelonephritis
Chronic pyelonephritis
Prerenal azotemia
Renal azotemia
Acute tubular necrosis
Postrenal azotemia
Renal papillary necrosis
Renal cortical necrosis
Chronic kidney disease
Polycystic kidney disease
Multicystic dysplastic kidney
Medullary cystic kidney disease
Medullary sponge kidney
Renal artery stenosis
Renal cell carcinoma
Angiomyolipoma
Nephroblastoma (Wilms tumor)
WAGR syndrome
Beckwith-Wiedemann syndrome
Posterior urethral valves
Hypospadias and epispadias
Vesicoureteral reflux
Bladder exstrophy
Urinary incontinence
Neurogenic bladder
Lower urinary tract infection
Transitional cell carcinoma
Non-urothelial bladder cancers
Congenital renal disorders: Pathology review
Renal tubular defects: Pathology review
Renal tubular acidosis: Pathology review
Acid-base disturbances: Pathology review
Electrolyte disturbances: Pathology review
Renal failure: Pathology review
Nephrotic syndromes: Pathology review
Nephritic syndromes: Pathology review
Urinary incontinence: Pathology review
Urinary tract infections: Pathology review
Kidney stones: Pathology review
Renal and urinary tract masses: Pathology review
Osmotic diuretics
Carbonic anhydrase inhibitors
Loop diuretics
Thiazide and thiazide-like diuretics
Potassium sparing diuretics
ACE inhibitors, ARBs and direct renin inhibitors
Endocrine system anatomy and physiology
Hunger and satiety
Insulin
Glucagon
Somatostatin
Diabetes mellitus
Diabetic retinopathy
Pancreatic neuroendocrine neoplasms
Parathyroid disorders and calcium imbalance: Pathology review
Diabetes insipidus and SIADH: Pathology review
Hyperthyroidism medications
Hypothyroidism medications
Insulins
Hypoglycemics: Insulin secretagogues
Miscellaneous hypoglycemics
Diabetes mellitus: Pathology review
Prostatitis
Prostate disorders and cancer: Pathology review
Prostate cancer
Prostate gland histology
Androgens and antiandrogens
PDE5 inhibitors
Adrenergic antagonists: Alpha blockers
Hyperthyroidism
Graves disease
Thyroid eye disease (NORD)
Toxic multinodular goiter
Thyroid storm
Euthyroid sick syndrome
Thyroid hormones
Hashimoto thyroiditis
Subacute granulomatous thyroiditis
Hypothyroidism
Thyroglossal duct cyst
Riedel thyroiditis
Thyroid cancer
Congenital adrenal hyperplasia
Primary adrenal insufficiency
Waterhouse-Friderichsen syndrome
Hyperaldosteronism
Adrenal cortical carcinoma
Cushing syndrome
Conn syndrome
Hyperparathyroidism
Hypoparathyroidism
Hyperpituitarism
Pituitary adenoma
Hyperprolactinemia
Prolactinoma
Gigantism
Acromegaly
Hypopituitarism
Pituitary apoplexy
Sheehan syndrome
Hypoprolactinemia
Constitutional growth delay
Diabetes insipidus
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Precocious puberty
Delayed puberty
Premature ovarian failure
Polycystic ovary syndrome
Androgen insensitivity syndrome
Kallmann syndrome
5-alpha-reductase deficiency
Autoimmune polyglandular syndrome type 1 (NORD)
Multiple endocrine neoplasia
Zollinger-Ellison syndrome
Carcinoid syndrome
Pheochromocytoma
Neuroblastoma
Opsoclonus myoclonus syndrome (NORD)
Adrenal insufficiency: Pathology review
Adrenal masses: Pathology review
Hyperthyroidism: Pathology review
Hypothyroidism: Pathology review
Thyroid nodules and thyroid cancer: Pathology review
Cushing syndrome and Cushing disease: Pathology review
Pituitary tumors: Pathology review
Hypopituitarism: Pathology review
Multiple endocrine neoplasia: Pathology review
Adrenal hormone synthesis inhibitors
Mineralocorticoids and mineralocorticoid antagonists
Synthesis of adrenocortical hormones
Cortisol
Testosterone
Estrogen and progesterone
Parathyroid hormone
Calcitonin
Adrenocorticotropic hormone
Growth hormone and somatostatin
Oxytocin and prolactin
Pituitary gland histology
Pancreas histology
Thyroid and parathyroid gland histology
Adrenal gland histology
Iron deficiency anemia
Alpha-thalassemia
Beta-thalassemia
Sideroblastic anemia
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Anemia of chronic disease
Lead poisoning
Hemolytic disease of the newborn
Autoimmune hemolytic anemia
Pyruvate kinase deficiency
Paroxysmal nocturnal hemoglobinuria
Hereditary spherocytosis
Sickle cell disease (NORD)
Fanconi anemia
Megaloblastic anemia
Folate (Vitamin B9) deficiency
Aplastic anemia
Vitamin B12 deficiency
Diamond-Blackfan anemia
Acute intermittent porphyria
Porphyria cutanea tarda
Hemophilia
Vitamin K deficiency
Hemolytic-uremic syndrome
Bernard-Soulier syndrome
Glanzmann's thrombasthenia
Immune thrombocytopenia
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Von Willebrand disease
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Heparin-induced thrombocytopenia
Factor V Leiden
Protein C deficiency
Protein S deficiency
Antiphospholipid syndrome
Antithrombin III deficiency
Hodgkin lymphoma
Non-Hodgkin lymphoma
Chronic leukemia
Acute leukemia
Myelodysplastic syndromes
Polycythemia vera (NORD)
Myelofibrosis (NORD)
Essential thrombocythemia (NORD)
Leukemoid reaction
Langerhans cell histiocytosis
Multiple myeloma
Monoclonal gammopathy of undetermined significance
Waldenstrom macroglobulinemia
Mastocytosis (NORD)
Microcytic anemia: Pathology review
Non-hemolytic normocytic anemia: Pathology review
Intrinsic hemolytic normocytic anemia: Pathology review
Extrinsic hemolytic normocytic anemia: Pathology review
Macrocytic anemia: Pathology review
Heme synthesis disorders: Pathology review
Coagulation disorders: Pathology review
Platelet disorders: Pathology review
Mixed platelet and coagulation disorders: Pathology review
Thrombosis syndromes (hypercoagulability): Pathology review
Lymphomas: Pathology review
Leukemias: Pathology review
Plasma cell disorders: Pathology review
Myeloproliferative disorders: Pathology review
Anticoagulants: Heparin
Anticoagulants: Warfarin
Anticoagulants: Direct factor inhibitors
Antiplatelet medications
Thrombolytics
Hematopoietic medications
Ribonucleotide reductase inhibitors
Topoisomerase inhibitors
Platinum containing medications
Anti-tumor antibiotics
Microtubule inhibitors
DNA alkylating medications
Monoclonal antibodies
Antimetabolites for cancer treatment
Anatomy of the thyroid and parathyroid glands
Pharyngeal arches, pouches, and clefts
Blood histology
Blood components
Blood groups and transfusions
Platelet plug formation (primary hemostasis)
Coagulation (secondary hemostasis)
Role of Vitamin K in coagulation
Clot retraction and fibrinolysis
Anatomy clinical correlates: Other abdominal organs
Anatomy of the male urogenital triangle
Membranoproliferative glomerulonephritis
von Hippel-Lindau disease
Klinefelter syndrome
Turner syndrome
Benign prostatic hyperplasia
Cryptorchidism
Varicocele
Orchitis
Testicular cancer
Epididymitis
Testicular torsion
Priapism
Penile cancer
Urethritis
Proteus mirabilis
Testicular tumors: Pathology review
Kidney stones: Clinical
Renal cysts and cancer: Clinical
Testicular and scrotal conditions: Pathology review
Anatomy clinical correlates: Inguinal region
Blood products and transfusion: Clinical
Venous thromboembolism: Clinical
Hypernatremia: Clinical
Hyponatremia: Clinical
Hyperkalemia: Clinical
Hypokalemia: Clinical
Metabolic and respiratory acidosis: Clinical
Metabolic and respiratory alkalosis: Clinical
Acute kidney injury: Clinical
Transplant rejection
Graft-versus-host disease
Cytomegalovirus infection after transplant (NORD)
Post-transplant lymphoproliferative disorders (NORD)
Rhabdomyolysis

Transcript

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Sheehan syndrome, also known as postpartum pituitary gland necrosis, was first described in the 1930s by British doctor and pathologist Harold Sheehan. In postpartum pituitary gland necrosis, “postpartum” means after childbirth; “pituitary gland” refers to a small, powerful gland that helps control hormones during pregnancy and beyond; while “necrosis” means cell death. So, in postpartum pituitary gland necrosis, parts or sometimes the entire pituitary gland can be damaged after childbirth, usually due to severe blood loss during or after delivery.

The pituitary gland sits in a small space at the base of the brain called the sella turcica, and it acts as the body's hormone control center. The front part, called the anterior pituitary gland, produces growth hormone, which helps the body grow; prolactin, which stimulates mammary glands to produce milk; as well as follicle-stimulating hormone and luteinizing hormone, which control menstrual cycle and fertility. Additionally, the anterior part produces thyroid-stimulating hormone, which keeps the metabolism running flawlessly, and adrenocorticotropic hormone, which stimulates the adrenal glands to produce cortisol. On the other hand, the back part, called the posterior pituitary gland, stores and releases two main hormones. One is the antidiuretic hormone, which controls the water balance in the body, and the second is oxytocin, which plays a key role in labor and contractions of the womb during childbirth.

During pregnancy, the pituitary gland works overtime to support the body through pregnancy and get it ready for childbirth and breastfeeding. One specific group of cells in the anterior pituitary, called lactotrophs, starts to grow in size and increase in number. These cells are responsible for prolactin production. As the lactotrophs grow and become more active, the pituitary gland grows, demanding more energy and resources. But here’s the catch. Even though the lactotrophs are growing, working harder, and using more energy, the blood supply to the pituitary gland doesn’t increase.

This makes the pituitary gland extremely vulnerable to blood loss. So, if there’s heavy bleeding during or after delivery, referred to as postpartum hemorrhage, the overall blood volume in the cardiovascular system drops, resulting in hypoperfusion of organs, including the brain and pituitary gland.

When the pituitary gland doesn’t get enough blood, it can’t get the oxygen and nutrients it needs, especially when it is already larger in size than usual. And lactotrophs, which are the most active cells, suffer the most. Without enough oxygen and nutrients, they die off, stopping prolactin production. This lack of blood flow that results in cell death is also known as ischemic necrosis and mainly affects the anterior pituitary gland.

If the body fails to restore blood flow quickly, damage to the pituitary gland can worsen. Over time, the pituitary gland can shrink and stop producing other hormones. In the most severe cases, it can become so small that it almost disappears from its spot in the skull. This condition is called empty sella turcica.

Now, switching gears and moving on to clinical manifestations. In rare cases, Sheehan syndrome shows up days or weeks after childbirth. But more often, signs and symptoms develop slowly over many years, which makes them easy to miss. And based on how much the pituitary gland is damaged, clinical features can vary from mild to severe.

In milder cases, the pituitary gland stops producing just one hormone, which is known as isolated hypopituitarism. Because lactotrophs are first to die off, the gland stops producing prolactin. With no prolactin, the body cannot trigger mammary glands to produce milk, which results in failure of lactation after delivery.

Key Takeaways

Sheehan syndrome, also known as postpartum hypopituitarism, is a condition that affects women who have experienced postpartum hemorrhage (PPH). PPH causes ischemia to lactotrophs and other cells of the pituitary, causing them. This results in deficiencies of prolactin, growth hormone, thyroid stimulating hormone, adrenocorticotropic hormone, luteinizing hormone, and follicle-stimulating hormone.

During pregnancy, pituitary cells increase in size and number, taking up more blood than usual. So, when there is PPH, these cells are prone to starve and become ischemic. An early symptom of Sheehan syndrome is agalactorrhea, whereas late symptoms include amenorrhea, low blood pressure, low blood sodium, and glucose levels, fatigue, and muscle loss. Sheehan's syndrome can be treated by replacing the deficient hormones, usually for a person's entire life.

Sources

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  2. "USMLE Step 1 Secrets in Color. Available from: ClinicalKey Student, (5th Edition). Page 167 " Elsevier Limited (UK) (2022)
  3. "Davidson's Principles and Practice of Medicine. Available from: ClinicalKey Student, (24th Edition). Page 694 " Elsevier Limited (UK) (2022)
  4. "Sheehan syndrome: a current approach to a dormant disease. 2025;28(1):20. " Pituitary (2025 Jan 25)
  5. "Sheehan syndrome. 2016;2:16092. " Nat Rev Dis Primers (2016 Dec 22)