Skip to main content
Clinical Case Reports logoLink to Clinical Case Reports
. 2021 Jun 24;9(6):e04315. doi: 10.1002/ccr3.4315

May‐Thurner syndrome: A cause of unexplained unilateral leg edema

Masaki Tago 1,, Motoshi Fujiwara 1, Yoshinori Tokushima 1, Shun Yamashita 1, Hidetoshi Aihara 1
PMCID: PMC8223893  PMID: 34194802

Abstract

Physicians should be familiar with May‐Thurner syndrome, characterized by the compression of the left common iliac vein by the right common iliac artery and the vertebral body, resulting in pain and swelling of the left lower extremity and DVT. A 64‐year‐old woman presented with unexplained edema in the left lower extremity. Computed tomography with contrast enhancement revealed that the left common iliac vein was compressed and narrowed by the right common iliac artery and the vertebral body, leading to the diagnosis of May‐Thurner syndrome.

Keywords: deep venous thrombosis, leg edema, May‐Thurner syndrome


Physicians should be familiar with May‐Thurner syndrome, characterized by the compression of the left common iliac vein by the right common iliac artery and the vertebral body, resulting in pain and swelling of the left lower extremity and DVT.

graphic file with name CCR3-9-e04315-g001.jpg

1. CASE

A 64‐year‐old woman presented with edema in the left lower extremity for 2 months. She was referred to our hospital because a diagnosis could not be made via ultrasonography. Her body mass index was 33 kg/m2, and physical examination revealed indurated edema in her left lower leg, without warmth or tenderness. Blood examination revealed no inflammatory reaction, and urinalysis, chest X‐ray, and electrocardiography revealed normal renal function, albumin, thyroid function, D‐dimer, and no abnormalities. Lymphoscintigraphy revealed no lymphatic vessel obstruction. Computed tomography with contrast enhancement revealed that the left common iliac vein was compressed and narrowed by the right common iliac artery and the vertebral body, leading to the diagnosis of May‐Thurner syndrome (MTS) (Figure 1, Video S1).

FIGURE 1.

FIGURE 1

Findings of abdominal computed tomography with contrast enhancement. Computed tomography with contrast enhancement revealed that the left common iliac vein was compressed (A, black arrows) by the right common iliac artery (A, white arrowhead) and the lumbar vertebral body. The distal part of the left internal iliac vein was dilated (B, white arrow)

May‐Thurner syndrome, wherein the left common iliac vein is compressed by the right common iliac artery and the vertebral body, is clinically significant because it causes pain and swelling of the left lower extremity, venous claudication, and deep venous thrombosis (DVT). 1 Female sex with postpartum, multiparity, oral contraceptives, scoliosis, dehydration, and hypercoagulable disorders is at high risk for MTS. 2 MTS was found in 14%–32% cases among unselected autopsies, suggesting that there are many undiagnosed cases. 1 Physicians should be familiar with MTS and correctly diagnose it in cases with edema or DVT in the left lower extremity without any cause or predisposing factors.

CONFLICT OF INTEREST

None declared.

AUTHOR CONTRIBUTIONS

MT: involved in literature search, concept, and drafting. MF: involved in literature search, drafting, and clinical care of the patient. YT, SY, HA: involved in conception and revision of the manuscript.

ETHICAL APPROVAL AND INFORMED CONSENT

The patient gave permission for the publication of this case report. This manuscript conforms to the provisions of the Declaration of Helsinki in 1995 (as revised in Brazil 2013).

Supporting information

Video S1

ACKNOWLEDGMENTS

We thank Edanz Group (https://en‐author‐services.edanz.com/ac) for editing a draft of this manuscript.

Tago M, Fujiwara M, Tokushima Y, Yamashita S, Aihara H. May‐Thurner syndrome: A cause of unexplained unilateral leg edema. Clin Case Rep. 2021;9:e04315. 10.1002/ccr3.4315

DATA AVAILABILITY STATEMENT

The data that support the findings of this study are available from the corresponding author upon reasonable request.

REFERENCES

  • 1. Harbin MM, Lutsey PL. May‐Thurner syndrome: history of understanding and need for defining population prevalence. J Thromb Haemost. 2020;18(3):534‐542. 10.1111/jth.14707 [DOI] [PubMed] [Google Scholar]
  • 2. Hng JZK, Su S, Atkinson N. May‐Thurner syndrome, a diagnosis to consider in young males with no risk factors: a case report and review of the literature. J Med Case Rep. 2021;15(1):141. 10.1186/s13256-021-02730-8 [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Video S1

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.


Articles from Clinical Case Reports are provided here courtesy of Wiley

RESOURCES