DOI:10.2214/AJR.07.3679
AJR 2008; 191:W71
© American Roentgen Ray Society
Uterine Diverticula and Accessory Ducts
Peter Evan and
Beverley Kramer
Netcare Park Lane Clinic Johannesburg, Republic of South
Africa
University of Witwatersrand Johannesburg, Republic of South
Africa
WEB—This is a Web exclusive article.
Our patient is a 34-year-old woman investigated for secondary infertility.
She has two children born by uncomplicated vaginal delivery. The patient has
no history of surgery, trauma, or pelvic infection. Hysterosalpingography
revealed an anteflexed uterus. Both fallopian tubes were normal. An additional
tubular structure arising from the left side of the uterus at the junction of
the body and cervix was noted (Figs.
1A and
1B). Two small diverticula were
seen on the right.
In our opinion, these findings are a developmental anomaly, not an acquired
condition. We consider this to be a true duplication (splitting) of either
mesonephric or paramesonephric duct. We use the term mesonephric for Wolffian
and paramesonephric for müllerian ducts, as preferred by embryologists.
The splitting occurs at the 7th week
[1]. The division may be short,
or it may be extensive and bilateral
[1]. The duplicated
paramesonephric duct runs parallel to the normal tube and may fuse with it on
one or both ends. In the radiologic literature
[2], the duplication of the
paramesonephric duct means either failure of fusion (types II, III, IV) or
failure of septal resorption (types V or VI). True duplications of the
mesonephric and paramesonephric ducts are not mentioned.
Clinical manifestations include incidental findings, as in our case;
parauterine pelvic mass; uterine diverticula; accessory or rudimentary horn of
the uterus; accessory tube; renal and ureteric abnormalities; or a combination
of these. Mesonephric and paramesonephric duct duplications may coexist in the
same patient. Histology will differentiate between the two.
Cervical diverticula are occasionally seen, but true uterine diverticula
are extremely rare in nonpregnant women
[3]. They represent localized
duplication of the distal paramesonephric duct and may mimic uterine
sacculation of pregnancy. Most of the accessory diverticula and tubes are a
portion of the epoophoron, which is a mesonephric duct remnant
[1]. The most common
complications are dysmenorrhea, infection, and ectopic pregnancy. Ectopic
pregnancy may mimic abdominal pregnancy, has a 70% chance of rupture, and does
not respond to induction of labor. Saharan and Parulekar
[4] described a patient with a
rudimentary horn of the uterus and an anomalous tubular structure on the
right, where a normal ureter is expected. The right kidney and ureter were
absent. The diagnosis of persistent mesonephric duct was confirmed at surgery
and by biopsy.
Our presentation has two drawbacks. First, the status of the right kidney
and ureter are unknown because evaluation of the urinary tract was not done.
Second, there was neither surgical nor biopsy correlation because these were
not indicated. True duplications are documented in the anatomic, pathologic,
surgical, and gynecologic literature, but we did not find any references in
the available English-language radiologic literature. The diverticula and
accessory duct are compatible with both mesonephric and paramesonephric duct.
On the basis of the course of the additional tube, we believe that our case is
a true duplication of the mesonephric duct.
References
- Gray SW, Skandalakis JE. Embryology for surgeons.
Philadelphia, PA: W. B. Saunders, 1972:596
-597, 640, 651
- Troiano RN, McCarthy SM. Mullerian duct anomalies: imaging and
clinical issues. Radiology 2004;233
: 19-34[Abstract/Free Full Text]
- Engel G, Rushovich AM. True uterine diverticulum. A partial
mullerian duplication? Arch Pathol Lab Med1984; 108:734
-736[Medline]
- Saharan SP, Parulekar SV. Hemihaematometra with persistent
underdevelped Wolffian duct. J Posgrad Med (serial
online) 1993 (cited 2007 Dec 19); 39:98
.
http://www.jpgmonline.com/text/asp?1993/39/2/98/623

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