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| Uterine malformation Classification & external resources | |
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| A human bicornuate uterus | |
| ICD-10 | Q51. |
| ICD-9 | 752.2-752.3 |
A uterine malformation is the result of an abnormal development of the Mullerian duct(s) during embryogenesis. Symptoms range from amenorrhea, infertility and pain, to normal functioning depending on the nature of the defect. Uterine malformations affect about 1% of the female population.
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The American Fertility Society (now American Society of Reproductive Medicine) Classification distinguishes:
A uterine septum can be corrected by hysteroscopic surgery.
An additional variation is the arcuate uterus where there is a concave dimple in the uterine fundus within the cavity.
A rudimentary uterus is a uterine remnant not connected to cervix and vagina and may be found on the other side of an unicornuate uterus.
Patients with uterine abnormalities may have associated renal abnormalities including unilateral renal agenesis.Li S, Qayyum A, Coakley FV, Hricak H. Association of renal agenesis and mullerian duct anomalies. J Comput Assist Tomogr. 2000 Nov-Dec;24(6):829-34. PMID 11105695
Uterine Didelphys is a rare type of deformity (1 in 1000 women) in the female reproductive organs in which some organs may be either split or duplicated. Typically, some of these "extra" organs are non-functional or semi-functional appendages, although on occasion they will be completely functional in all normal respects, and often independently. As the vagina is largely derived from the Mullerian ducts, lack of fusion of the two ducts can lead to the formation of a vaginal septum, or "double vagina", a condition sometimes called with a uterus didelphys or a uterine septum.Heinonen PK.Complete septate uterus with longitudinal vaginal septum. Fertil Steril. 2006 Mar;85(3):700-5. PMID 16500341Perez-Brayfield MR,Clarke HS,Pattara JG. Complete bladder, urethral, and vaginal duplication in a 50-year-old woman. Urology. 2002 Sep;60(3):514. PMID 12350504British Woman With 2 Wombs Has Triplets. Associated Press, 22 Dec. 2006.
Besides a physical examination, the physician will need imaging techniques to determine the character of the malformation: gynecologic ultrasonography, pelvic MRI, or hysterosalpingography. A hysterosalpingogram is not considered as useful due to the inability of the technique to evaluate the exterior contour of the uterus and distinguish between a bicornuate and septate uterus. In addition, laparoscopy and/or hysteroscopy may be indicated. In some patients the vaginal development may be affected.
Surgical intervention depends on the extent of the individual problem. With a didelphic uterus surgery is not usually recommended. A uterine septum can be resected in a simple out-patient procedure that combines laparoscopy and hysteroscopy. This procedure greatly decreases the rate of miscarriage for women with this anomaly.
| Congenital malformations and deformations of genital organs and urinary system (Q50-Q64, 752-753) | |
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| Genital organs (overview) | female: Uterine malformation - Mullerian agenesis - Uterine didelphys - Clitoromegaly
male: Cryptorchidism - Hypospadias - Chordee - Monorchism - Micropenis - Penile agenesis Pseudohermaphroditism |
| Urinary system | kidney/ureter: Renal agenesis/Potter syndrome - cystic (Polycystic kidney disease, Meckel syndrome, Multicystic dysplastic kidney) - Ectopic ureter - Horseshoe kidney - Renal ectopia
bladder/urethra: Epispadias - Bladder exstrophy urachus: Urachal cyst |
| See also non-congenital reproductive and urinary conditions (N, 580-629) | |
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