Amenorrhea resident survival guide

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For details about amenorrhea click here.

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Eiman Ghaffarpasand, M.D. [2]

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Overview
Classification
Causes
FIRE
Diagnosis
Treatment
Do's
Don'ts

Overview

The first descriptions about disturbances in menstrual cycle are found in Papyrus Ebres [named after the Egyptologist Georg M. Ebers (1837-1898)], from New Kingdom period (1450-1550 B.C.E). Amenorrhea may be classified according to etiology into three subtypes, including primary amenorrhea, secondary amenorrhea, and functional amenorrhea. Primary amenorrhea is basically refers to a young girl who have not experienced menarche, at all. Secondary amenorrhea reflects a woman who had normal menstruation cycles, experiencing at least 3 months of absence of menstruation cycle . Functional amenorrhea is a subtype of the amenorrhea caused by exaggerated different lifestyles. Primary and secondary amenorrhea are distinguished solely based on history. The pathophysiology of amenorrhea is described in many categories, include hypothalamic, pituitary, thyroid, adrenal, ovarian, uterine, and vaginal pathogenesis. About 25 various genes, in 3 different group of Kallmann syndrome related genes, hypothalamus-pituitary-gonadal (HPG) axis related genes, and obesity related genes, play roles in amenorrhea. Common causes of amenorrhea include breastfeeding, pregnancy, menopause, and stress. Primary amenorrhea must be differentiated from other diseases that cause lack of menstrual cycle, such as Mullerian agenesis, 3-beta-hydroxysteroid dehydrogenase type 2 deficiency, androgen insensitivity syndrome, Kallmann syndrome, Turner syndrome, and 17-alpha-hydroxylase deficiency. In contrast, secondary amenorrhea must be differentiated from other diseases that cause menstrual cycle arrest, such as primary ovarian insufficiency, hypothyroidism, hyperprolactinemia, polycystic ovary syndrome, and Asherman's syndrome. The prevalence of amenorrhea is approximately 3,000 to 4,000 per 100,000 individuals worldwide. The most common risk factor in the development of primary amenorrhea is chromosomal disorder and the most common risk factor in the development of secondary amenorrhea is breastfeeding. If left untreated, all of patients with amenorrhea may progress to develop infertility and osteoporosis. Common complications of amenorrhea are based on the background disease that induced it. Prognosis is generally excellent and the mortality rate of patients with amenorrhea is approximately less than 1%, generally in patients with amenorrhea due to brain lesions. The initial laboratory tests for evaluating amenorrhea are pregnancy test, thyroid stimulating hormone (TSH), follicle stimulating hormone (FSH), and prolactin (PRL). Second line laboratory tests include free and total testosterone, dehydroepiandrosterone sulfate (DHEAS), and also progesterone challenge test. There are no echocardiography findings associated with amenorrhea. However, an echocardiography may be helpful in the diagnosis of the diseases that can cause amenorrhea, such as Turner syndrome. Findings on an echocardiography suggestive of Turner syndrome include bicuspid aortic valve, elongation of transverse aortic arch, coarctation of aorta, and partial anomalous pulmonary venous return (PAPVR). There are no ultrasound findings associated with amenorrhea. However, an ultrasound may be helpful in the diagnosis of the diseases that can cause amenorrhea, such as polycystic ovary syndrome (PCOS), premature ovarian insufficiency, androgen insensitivity syndrome, 17-alpha hydroxylase deficiency, and also anatomic genital defects. Pharmacologic medical therapy is recommended among patients with hypothalamic causes, pituitary causes, ovarian insufficiency, and chronic anovulation. The general principle of the treatment in amenorrhea is sex hormones replacement therapy, mostly with suitable forms of estrogen and progesterone. The mainstay of treatment for amenorrhea is medical therapy. Surgery is usually reserved for patients with either hypothalamus or pituitary tumors, Turner syndrome, and genital anatomical defects (imperforate hymen or transverse vaginal septum). The surgical treatment for hypothalamus or pituitary tumors is tumor resection via endoscopic transsphenoidal surgery. Ovaries have to be excised in Turner syndrome to prevent malignant transformation. Small incision is the main surgery for imperforate hymen and septal excision is the main treatment for transverse vaginal septum.

Classification

  • Amenorrhea may be classified according to etiology into three subtypes:
    • Primary amenorrhea
    • Secondary amenorrhea
    • Functional amenorrhea
  • Each of the subtypes of amenorrhea has their own classifications, as following:
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Amenorrhea classification
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Lifestyle etiology
 
 
 
 
 
 
 
 
 
 
Lack of menarche
 
 
 
 
 
 
 
 
 
 
 
 
Mensturation absence
more than 3 months
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Functional amenorrhea
 
 
 
 
 
 
 
 
 
 
Primary amenorrhea
 
 
 
 
 
 
 
 
 
 
 
 
Secondary amenorrhea
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Stress related
 
Weight loss related
 
Exercise related
 
Present uterus
 
 
 
 
 
 
 
Absent uterus
 
Polycystic ovary syndrome
 
Hypothalamic-pituitary dysfunction
 
Hypothalamic-pituitary failure
 
Ovarian failure
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Hypergonadotropic hypogonadism
 
Hypogonadotropic hypogonadism
 
Eugonadotropic
 
Mullerian agenesis
 
Androgen insensitivity
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Causes

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Amenorrhea causes
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Anatomic defects
Outflow obstruction
 
 
 
 
 
 
Primary hypogonadism
 
 
 
 
 
 
 
 
 
Hypothalamic causes
 
 
Pituitary causes
 
 
 
 
 
 
 
 
 
 
 
 
Other endocrine gland disorder
 
 
 
 
 
 
 
 
 
 
 
Multifactorial causes
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Gonadal dysgenesia
 
Gonadal agenesis
 
Enzymatic deficiency
 
Premature ovarian failure
 
Dysfunctional
 
Other disorders
 
 
 
 
Adrenal disease
 
Thyroid disease
 
Ovarian tumor
 
Mass lesion
 
Necrosis
 
Inflammatory/
Infiltrative
 
Gonadotropin mutations
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Mullerian agenesis(Mayer-Rokitansky-Kuster-Hauser syndrome)
• Complete androgen insensitivity syndrome (tesicular feminization)
• Intra-uterine synechiae (Asherman syndrome)
Imperforate hymen
• Transverse vaginal septum
Cervical agenesis-isolated
Cervical stenosis-iatrogenic
Vaginal agenesis- isolated
Endometrial hypoplasia or aplasia-congenital
 
1.Abnormal karyotype
Turner syndrome
Mosaicism
2.Normal karyotype (pure gonadal dysgenesis)
• 46, XX
• 46, XY (Swyer syndrome)
 
 
 
17 alpha hydroxylase deficiency
• 17,20-Lyase deficiency
Aromatase deficiency
 
1.Idiopathic
2.Injury
Chemotherapy
Radiation
Mumps oophoritis
3.Resistant ovary
 
1.Stress
2.Exercise
3.Nutrition-related
Weight loss, Diet, Malnutrition
Eating disorders (anorexia nervosa, bulimia)
4.Pseudocyesis
 
1. Isolated gonadotropin deficiency
Kallmann syndrome
• Idiopathic hypogonadotropic hypogonadism
2. Infection
Tuberculosis
Syphilis
Encephalitis
Meningitis
Sarcoidosis
3. Chronic debilitating disease
4.Tumors
Craniopharyngioma
Germinoma
Hamartoma
Langerhans cell histiocytosis
Teratoma
Endodermal sinus tumor
Metastatic carcinoma
 
1.Prolactinoma
2. Other hormones secreting pituitary tumors
3. Mutations of FSH receptors
4. Mutations of LH receptors
5.Autoimmune disease
6.Galactosemia
 
Adrenal hyperplasia
Cushing syndrome
 
Hypothyroidism
Hyperthyroidism
 
Granulosa-theca cell tumor
Brenner tumor
Cystic teratoma
Mucinous cystadenoma
Krukenberg tumors
Craniopharyngioma
Metastatic carcinoma
 
Empty sella
Arterial aneurysm
 
Sheehan syndrome
Panhypopituitarism
 
Sarcoidosis
Hemochromatosis
Lymphocytic hypophysitis
 
 
Polycystic ovary syndrome

FIRE: Focused Initial Rapid Evaluation

Diagnosis

Treatment

Do's

Dont's

References