AJR 2005; 184:703-704
© American Roentgen Ray Society
Thrombosed Pelvic Collateral Veins Resulting from Anomalous Inferior Vena Cava: A Mimicker of Acute Appendicitis
Fenella J. Moulding1,
Sue C. Roach1 and
Anthony E. Hanbidge1
1 University Health Network and Mount Sinai Hospital University of
Toronto Toronto, ON M5G 2N2, Canada
A 22-year-old man with a history of congenital heart disease presented with
right lower quadrant pain and tenderness. Sonography showed a noncompressible,
tubular, predominantly hypoechoic structure at the region of maximal
tenderness. A trace of free fluid and echogenic inflammatory fat was seen
surrounding this structure (Figs.
2A and
2B). No Doppler flow was
detected in this structure on sonography.

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Fig. 2A. 22-year-old man with infrarenal absence of inferior vena cava
and thrombosis of right pelvic collateral vein mimicking acute appendicitis.
Sagittal (A) and transverse (B) sonograms show distended,
noncompressible tubular structure (arrow) in right lower quadrant.
Note adjacent inflammatory echogenic fat and small amount of free fluid.
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Fig. 2B. 22-year-old man with infrarenal absence of inferior vena cava
and thrombosis of right pelvic collateral vein mimicking acute appendicitis.
Sagittal (A) and transverse (B) sonograms show distended,
noncompressible tubular structure (arrow) in right lower quadrant.
Note adjacent inflammatory echogenic fat and small amount of free fluid.
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The diagnosis of acute appendicitis was considered, although two features
were not entirely in keeping with this. First, a communication between the
tubular structure and the cecum could not be visualized. Second, a definite
blind end could not be identified. We thought that if the appendix had
ruptured, then such features might be absent.
Because the sonographic diagnosis was uncertain, MDCT was performed. The
patient refused IV contrast material. MDCT revealed a distended, hyperdense
right pelvic collateral vein with surrounding fat stranding and free fluid
(Fig. 2C). The inferior vena
cava was anomalous, with normal preservation of the suprarenal portion but
absence of the infrarenal portion (Fig.
2D). In addition, both common iliac veins were absent. On the
left, the external and internal iliac veins fused to form an enlarged
ascending lumbar vein, draining blood from the lower limbs to the suprarenal
inferior vena cava. On the right, prominent collateral veins were present in
the groin, and the enlarged hyperdense tortuous collateral vein was seen to
communicate with the right ascending lumbar vein
(Fig. 2E).

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Fig. 2C. 22-year-old man with infrarenal absence of inferior vena cava
and thrombosis of right pelvic collateral vein mimicking acute appendicitis.
Unenhanced CT image shows distended, tortuous, hyperdense, thrombosed venous
collateral vessel (arrow) with surrounding inflammatory change.
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Fig. 2D. 22-year-old man with infrarenal absence of inferior vena cava
and thrombosis of right pelvic collateral vein mimicking acute appendicitis.
Unenhanced CT image shows absence of infrarenal inferior vena cava. Note
presence of normal aorta (arrow).
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Fig. 2E. 22-year-old man with infrarenal absence of inferior vena cava
and thrombosis of right pelvic collateral vein mimicking acute appendicitis.
Unenhanced CT image shows dilated ascending lumbar veins (arrowheads)
that drain blood from lower limbs. Note normal common iliac arteries
(arrows) but absence of common iliac veins.
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The findings are those of thrombophlebitis of a right pelvic collateral
vein. MDCT performed 1 year previously confirmed the anomalous anatomy but
absence of the thrombosis. Further Doppler sonography was performed to
evaluate the veins of both legs. The collateral venous channels in the right
groin were patent, but no normal common femoral vein was seen. The superficial
femoral and popliteal veins were patent. The left common femoral, superficial
femoral, and popliteal veins were also patent.
Deep venous thrombosis is a recognized complication of inferior vena cava
anomalies. Such anomalies should therefore be suspected in all cases of deep
vein thrombosis, especially if bilateral, in young patients
[1]. Venous stasis due to
inadequate venous return despite prominent collateral vessels has been
postulated as a possible mechanism of thrombosis in such cases
[1]. A few reports exist of
ovarian vein thrombosis mimicking appendicitis on helical CT and sonography
[2,
3], but we found no other
reports of an anomalous inferior vena cava with thrombosis of a collateral
vessel mimicking appendicitis. In this case, the presence of a tender,
noncompressible tubular structure in the right iliac fossa with surrounding
free fluid and inflammatory fat was suspected to be acute appendicitis. The
absence of some cardinal features of appendicitis, such as a blind-ending tube
and connection with the cecum, made a definitive diagnosis on sonography
difficult [4]. In such cases it
may be prudent to perform helical CT, which in this case revealed pelvic
venous thrombosis mimicking appendicitis. Obviously the treatment is
completely different for these two entities. The patient avoided unnecessary
surgery and was treated conservatively with anticoagulants.
References
- Gayer G, Luboshitz J, Hertz M, et al. Congenital anomalies of the
inferior vena cava revealed on CT in patients with deep venous thrombosis.
AJR 2003;180:729
732[Abstract/Free Full Text]
- Van Hoe L, Baert AL, Marchal G, Spitz B, Penninckx F. Thrombosed
ovarian vein collateral mimicking acute appendicitis on CT. J
Comput Assist Tomogr 1994;18:643
646[Medline]
- Adkins J, Wilson S. Unusual course of the gonadal vein: a case
report of post-partum ovarian vein thrombosis mimicking acute appendicitis
clinically and sonographically. J Ultrasound Med1996; 15:409
412[Medline]
- Birnbaum BA, Wilson SR. Appendicitis at the millennium.
Radiology2000; 215:337
348[Abstract/Free Full Text]

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