Tlili Yassine, Hadrich Zied, Hafsi Montacer, Sahir Omrani, Rached Bayar, Mestiri Hafedh
Department of General Surgery, Mongi Slim University Hospital, Faculty of Medicine of Tunis, Tunisia.
Department of General Surgery, Mongi Slim University Hospital, Faculty of Medicine of Tunis, Tunisia.
Int J Surg Case Rep. 2024 Mar;116:109414. doi: 10.1016/j.ijscr.2024.109414. Epub 2024 Feb 23.
Chylous ascites is an uncommon form of ascites characterized by milky fluid rich in triglycerides. It is associated with poor lymphatic drainage. We report a case of chylous ascites revealing a follicular lymphoma.
A 73-year-old man presented with a 6-month history of abdominal distension attributed to a chylous ascitis. The thoraco-abdomino-pelvic CT scan revealed voluminous intra- and retroperitoneal mass inseparable from the duodeno-pancreatic block and encompassing the mesenteric vessels, inferior vena cava and renal vessels; abundant ascites and multiple mediastinal, coeliomesenteric, retroperitoneal, iliac and inguinal adenomegalia. The diagnosis of follicular lymphoma was retained through a radio-guided biopsy of the retroperitoneal mass. The patient had weekly paracentesis and immuno-chemotherapy. The course was unfavorable, marked by infection of the ascites fluid after two cycles of immuno-chemotherapy. Our patient developed severe sepsis and died.
Chylous ascites in conjunction with follicular lymphoma is an exceptional presentation. The pathophysiological mechanism is an impediment to subdiaphragmatic lymphatic drainage caused by external pressure, leading to leakage of dilated subserosal lymphatic ducts into the peritoneal cavity. Histological confirmation is fundamental to manage chylous ascites resulting from lymphomas.
Chylous ascites revealing lymphoma is a unique condition. The key to management is the treatment of the underlying etiology.
乳糜性腹水是一种罕见的腹水形式,其特征为富含甘油三酯的乳状液体。它与淋巴引流不畅有关。我们报告一例乳糜性腹水病例,该病例确诊为滤泡性淋巴瘤。
一名73岁男性患者,因乳糜性腹水出现腹胀6个月。胸腹盆腔CT扫描显示,大量腹腔内和腹膜后肿块与十二指肠胰腺肿块相连,包绕肠系膜血管、下腔静脉和肾血管;大量腹水以及多个纵隔、腹腔肠系膜、腹膜后、髂骨和腹股沟淋巴结肿大。通过对腹膜后肿块进行放射性引导活检确诊为滤泡性淋巴瘤。患者每周进行腹腔穿刺及免疫化疗。病情进展不利,在两个周期的免疫化疗后出现腹水感染。我们的患者发展为严重脓毒症并死亡。
乳糜性腹水合并滤泡性淋巴瘤是一种罕见的表现形式。其病理生理机制是由于外部压力导致膈下淋巴引流受阻,致使扩张的浆膜下淋巴管渗漏至腹腔。组织学确诊对于处理淋巴瘤所致的乳糜性腹水至关重要。
乳糜性腹水合并淋巴瘤是一种独特的病症。治疗的关键在于治疗潜在病因。