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Pseudo-Pseudo Meigs' Syndrome in a 40-Year-Old Woman Without a Prior Systemic Lupus Erythematosus Diagnosis.
Cureus
November 2024
Internal Medicine, Tbilisi State Medical University, Tbilisi, GEO.
Pseudo-pseudo Meigs' syndrome (PPMS), also known as Tjalma syndrome, is an exceptionally rare condition marked by pleural effusion, ascites, and elevated CA-125 levels, usually in the context of systemic lupus erythematosus (SLE) without any associated ovarian tumors. We report the case of a 40-year-old woman who presented with a four-month history of fatigue, nausea, weight loss, abdominal pain, and pleural effusion. Initial diagnostic workup revealed ascites, elevated CA-125 levels, and pleural effusions, with no evidence of malignancy.
View Article and Find Full Text PDFProtein-losing enteropathy as the first presentation of systemic lupus erythematosus the first case reported in Palestine with systemic review.
Ann Med Surg (Lond)
December 2024
Al- Ahli Hospital, Department of Internal Medicine, Hebron, State of Palestine.
Introduction: Systemic lupus erythematosus is a chronic inflammatory disease affecting women, causing gastrointestinal issues like acute pancreatitis, esophagitis, and protein-losing enteropathy. Protein loss is uncommon, but a case study shows protein-losing enteropathy as a first sign.
Importance: Protein-losing enteropathy (PLE) is a rare gastrointestinal manifestation of SLE, often seen years before diagnosis.
Meigs syndrome after treatment for catamenial pneumothorax.
Gen Thorac Cardiovasc Surg Cases
November 2023
Department of Surgery, Imamitsu Homecare Clinic, 1-9-10 Imamitsu, Wakamatsu-Ku, Kitakyushu, 808-0071, Japan.
Article Synopsis
- Catamenial pneumothorax (CP) is a rare condition affecting women, characterized by a collapsed lung associated with menstrual cycles, while Meigs syndrome (MS) involves benign ovarian tumors causing pleural effusion and ascites, and its exact causes are not well understood.
- A 40-year-old Japanese woman was diagnosed with CP after experiencing dyspnea and undergoing surgery that revealed diaphragmatic foramens.
- Ten years later, the same patient presented with chest pain and imaging showed signs of MS, leading to surgery that resolved her symptoms, highlighting the rare occurrence of both conditions in one patient and suggesting links between them.
Rare giant ovarian thecoma presented as atypical/incomplete Meigs' syndrome: A case image report.
Clin Case Rep
November 2024
Third Department of Obstetrics and Gynecology University General Hospital "ATTIKON", Medical School, National and Kapodistrian University of Athens Athens Greece.
We present a 39-centimeter thecoma with ascites and elevated Ca-125 values which is compatible with an atypical/incomplete Meigs' syndrome. Giant ovarian masses with elevated Ca-125 values and ascites are an alarming combination, although Gynecologists should be aware that there are also benign entities that mimic advanced stage ovarian cancer.
View Article and Find Full Text PDFAnticoagulation therapy for a rare case of pseudo-Meigs' syndrome complicated by massive ascites in the postpartum period.
J Int Med Res
October 2024
Department of Obstetrics and Gynecology, Women and Children's Hospital of Ningbo University, Ningbo, Zhejiang, China.
Article Synopsis
- - The case report discusses a postpartum woman suffering from pseudo-Meigs' syndrome (PMS) characterized by symptoms like abdominal pain, significant ascites, and hypercoagulation.
- - Treatment with emergency anticoagulation led to improvements, such as the resolution of ascites and abdominal pain, despite the presence of a large degenerating uterine fibroid.
- - Pathological analysis post-surgery confirmed the diagnosis, and ongoing research is recommended to explore the link between hypercoagulable states and PMS in pregnant patients.
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