Tripathi Mayank, Parshad Sanjeev, Karwasra Rajender Kumar, Gupta Ashish, Srivastva Saket, Sarwal Ankush
Department of Surgical Oncology, Ward Nos. 6 and 8, Unit 1, Pt.B.D.Sharma, PGIMS, Rohtak, Haryana 124001, India.
Department of Surgery, Pt.B.D.Sharma, PGIMS, Rohtak, Haryana 124001, India.
Case Rep Surg. 2015;2015:732531. doi: 10.1155/2015/732531. Epub 2015 Mar 17.
Background. Retroperitoneal lymphangioma is a rare, benign mesodermal tumor arising from the retroperitoneal lymphatics which usually presents in infancy and it is worthy to report a case when it has presented in an adult. After a thorough literature search in English we concluded that less than 200 cases of adult retroperitoneal lymphangioma have been reported so far. Apart from being a rare entity it also presents as a diagnostic dilemma and final diagnosis is often made on surgical exploration. Case Presentation. We report a case of retroperitoneal lymphangioma in a 55-year-old male who presented with abdominal distension and dull aching abdominal pain. Conclusion. Retroperitoneal lymphangiomas are rare tumors of infancy but may also present in adults where they are a diagnostic challenge. Differentiating cystic lymphangiomas from other cystic growths by imaging studies alone are often inconclusive and surgery is frequently required for definitive diagnosis and to ameliorate the symptoms.
背景。腹膜后淋巴管瘤是一种罕见的良性中胚层肿瘤,起源于腹膜后淋巴管,通常在婴儿期出现,而当其在成人中出现时值得报告一例。在对英文文献进行全面检索后,我们得出结论,迄今为止报道的成人腹膜后淋巴管瘤病例少于200例。除了是一种罕见的疾病外,它还表现为诊断难题,最终诊断往往通过手术探查做出。病例报告。我们报告一例55岁男性腹膜后淋巴管瘤病例,该患者表现为腹胀和腹部隐痛。结论。腹膜后淋巴管瘤是婴儿期罕见的肿瘤,但也可能出现在成人中,在成人中它们是诊断挑战。仅通过影像学研究将囊性淋巴管瘤与其他囊性肿物区分开来往往没有定论,通常需要手术来明确诊断并缓解症状。