Background: Intraperitoneal lymphangioma (IL) used to be thought of as a benign lymphatic malformation with a low rate of preoperative diagnosis. This retrospective study aimed to explore the connection between the cysts and clinical manifestation and imaging characteristics, and to study diagnostic confusion, therapeutic principles and potential recurrent reasons, to further enhance the comprehension of this rare disease.
Methods: Here, we retrospectively reviewed 21 patients diagnosed with IL. Age, sex, complaints, physical findings, and imaging features of each patient were documented. The therapies, postoperative complications and treatments were discussed.
Results: Symptomatology included eight patients (38%) with intermittent dull pain in the abdomen, and three patients (14%) complained of abdominal persistent pain. The physical examination revealed an abdominal mass in 16 patients (76%), and eight (38%) were reported no discomfort. IL was correctly established preoperatively in 19 patients (90%). Patients were treated using laparotomy, except one who was treated with laparoscopy. Two recurrences were noted during follow-up.
Conclusions: IL should be suspected in any patient with a mobile abdominal mass and surgery is required immediately after discovery of the tumor.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795246 | PMC |
http://dx.doi.org/10.4103/0366-6999.169061 | DOI Listing |
Pan Afr Med J
November 2024
Service de Chirurgie Générale et Oncologique, Centre Hospitalier Universitaire de Beni-Messous, Alger, Algérie.
Intraperitoneal Cystic Lymphangioma (CL) is a rare benign malformative disease of lymphatic origin, with a wide range of clinical symptoms. Diagnosis is based on imaging tests and confirmed by histology. We here report the case of a 54-year-old woman presenting with chronic abdominal pain, with no effect on general condition.
View Article and Find Full Text PDFCureus
May 2024
Surgical Oncology, Marshfield Medical Center, Marshfield, USA.
Benign multicystic peritoneal mesothelioma (BMPM), also known as multicystic peritoneal mesothelioma (MCPM), is a rare cystic neoplasm arising from the mesothelium lining of the abdominal and pelvic peritoneum. This entity has been disproportionately described in women of reproductive age. Both the etiology and pathogenesis of the condition are not well understood.
View Article and Find Full Text PDFInt J Surg Case Rep
September 2023
Pediatric Surgery, Faculty of Medicine, Assiut University, Egypt. Electronic address:
Introduction And Importance: Chylolymphatic cysts are benign pathology in lymphatic vessels due to obstruction in the lymphatic system. Their incidence is still unknown. However, they account for approximately 3 % to 9 % of all pediatric lymphangiomas.
View Article and Find Full Text PDFInt J Surg Case Rep
June 2023
Department of Surgery A La Rabta Hospital, Tunis, Tunisia; Faculty of Medicine of Tunis, Tunis El Manar University, Tunis, Tunisia.
Introduction And Importance: Benign multicystic peritoneal mesothelioma is rare, with around 200 cases reported in the literature. We report the case of a patient operated on for the diagnosis of cystic lymphangioma but the pathology examination retained the diagnosis of benign cystic peritoneal mesothelioma.
Case Presentation: A 47-year-old patient, who consulted for abdominal distension evolving for a year.
Int J Surg Case Rep
April 2023
Department of General Surgery, Imam Hosein Medical and Educational Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address:
Introduction And Importance: Mesenteric cystic lymphangioma (MCL) is a rare benign intraperitoneal mass with congenital origin, and it is extremely rare in adults. Mesentery is an unusual location for cystic lymphangioma too. Clinical presentations are nonspecific, and diagnosis is challenging.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!