# A Case of Atypical Meig’s Syndrome Presenting With Pleural and Pericardial Effusion

**Authors:** Marwa Mir, Bella A Gnakou, Hamid Shaaban, Gunwant Guron, Zafar Jamil

PMC · DOI: 10.7759/cureus.77976 · Cureus · 2025-01-25

## TL;DR

This paper describes a rare case of Meigs syndrome in an elderly woman with unusual pleural and pericardial effusions alongside a benign ovarian tumor.

## Contribution

The case highlights the atypical presentation of Meigs syndrome with concurrent pleural and pericardial effusions, which is exceptionally rare.

## Key findings

- A 75-year-old patient presented with a benign ovarian tumor, pleural effusion, and pericardial effusion, fulfilling the criteria for Meigs syndrome.
- The patient's condition was complicated by a femur fracture and microcytic anemia, adding diagnostic complexity.
- Imaging revealed a large ileal mass and fluid accumulation without ascites, challenging typical diagnostic expectations.

## Abstract

Meigs syndrome is a rare condition characterized by the triad of benign ovarian tumors, ascites, and pleural effusion. However, concurrent presentation with both pleural and pericardial effusions is exceedingly rare. This paper presents a unique case of Meigs syndrome in a 75-year-old African American female patient with a history of anemia who was admitted for a left femur fracture secondary to a fall.

In addition to her orthopedic injury, the patient exhibited intermittent abdominal fullness and discomfort, prompting a thorough diagnostic evaluation. Physical examination was unremarkable, and laboratory investigations revealed microcytic anemia with normal renal and hepatic function tests. Unexpectedly, imaging studies revealed the presence of a large lobulated enhancing mass lesion arising from the terminal ileum, with no evidence of ascites. Computed tomography (CT) imaging also revealed bilateral pleural effusions and a mild pericardial effusion. Initial diagnostic evaluations yielded no significant findings with normal CA-125 and CEA levels and no abnormalities in peripheral blood.

The pathophysiology underlying the development of pleural and pericardial effusions in Meigs syndrome remains unclear but is thought to involve lymphatic obstruction and increased vascular permeability secondary to the ovarian tumor.

In conclusion, this case underscores the importance of recognizing variant presentations of Meigs syndrome, particularly in the context of concurrent pleural and pericardial effusions, which may pose diagnostic challenges but warrant prompt identification and management to optimize patient outcomes.

## Linked entities

- **Diseases:** Meigs syndrome (MONDO:0017799), anemia (MONDO:0002280)

## Full-text entities

- **Genes:** CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, MUC16 (mucin 16, cell surface associated) [NCBI Gene 94025] {aka CA125}
- **Diseases:** anemia (MESH:D000740), Meig's Syndrome (MESH:D008539), orthopedic injury (MESH:D009140), lesion (MESH:D009059), Pleural and Pericardial Effusion (MESH:D010996), femur fracture (MESH:D000092524), benign ovarian tumors (MESH:D010051), pericardial effusion (MESH:D010490), microcytic anemia (MESH:C536357), Meigs syndrome (MESH:D008538), ascites (MESH:D001201), abdominal fullness (MESH:D000007), lymphatic obstruction (MESH:D008206)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC11849800/full.md

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Source: https://tomesphere.com/paper/PMC11849800