ISSN: 2455-5282
Global Journal of Medical and Clinical Case Reports
Case Report       Open Access      Peer-Reviewed

A giant abdominal well differentiated Liposarcoma: A rare etiology of abdominal mass

Soukaina EL Yazal1*, Abdelouahed Louzi2, Fatima Z Lairani1, Soukaina Jiddi1, Imane Haraki1, Sofia Oubaha3, Zouhour Samlani Sebbane1 and Khadija Krati1

1Department of Gastroenterology, Hospital of Erazi, CHU Mohamed VI, Marrakesh, Morocco
2Department of visceral surgery, Hospital of Erazi, CHU Mohamed VI, Marrakesh, Morocco
3Department of Physiology, Faculty of Medicine, Marrakesh, Morocco
*Corresponding author: Soukaina EL Yazal, Department of gastroenterology, Hospital of Erazi, CHU Mohamed VI, Marrakesh, Morocco. E-mail: soukainaelyazal@gmail.com
Received: 07 December, 2017 | Accepted: 30 January, 2018 | Published: 31 January, 2018
Keywords: Giant abdominal mass; Retroperitoneal mass; Encapsulated mass; Surgical resection; Liposarcoma

Cite this as

Yazal SEL, Louzi A, Lairani FZ, Jiddi S, Haraki I, et al. (2018) A giant abdominal well differentiated Liposarcoma: A rare etiology of abdominal mass. Glob J Medical Clin Case Rep 5(1): 001-002. DOI: 10.17352/2455-5282.000057

Liposarcoma is the most common retroperitoneal sarcoma and represents more than 15% of all sarcomas. Well differentiated liposarcoma is usually located in the extremities. We report the case of a patient with a giant retroperitoneal liposarcoma revealed by an abdominal mass.

Case presentation: A 67 years old woman is admitted to our hospital for abdominal distension and pain that has been evolving for 2 years. Medical examination revealed a huge abdominal mass. Computed tomography (CT) scan showed a giant retroperitoneal mass with regular borders, pressing back abdominal organs and encasing the right kidney evoking a very probable liposarcoma. The patient has thus undergone a surgical resection of the mass alongside with nephrectomy of the right kidney. Histological findings confirmed well differentiated liposarcoma. Postoperative follow up was simple and no recurrent tumor was identified. The only known effective treatment of well differentiated liposarcoma is the complete surgical resection.

Introduction

Liposarcoma is the most common retroperitoneal sarcoma and represents more than 15% of all sarcomas. Several subtypes are described, based on histology, cytogenetic and molecular analysis [1]. Well-Differentiated Liposarcoma (WDL), called also Atypical Lipomatous Neoplasm (ALN), are the most common of liposarcomas, usually developed in the deep muscles of the extremities (75%), less frequently , in retroperitoneum (20%) [2]. we report in this case a giant form of retroperitoneal liposarcoma, encasing the kidney and treated successfully by surgical resection.

Case Report

A 67 years old woman, on her medical history, we noted hypertension and psoriasis, was admitted to our hospital for distension and abdominal pain evolving 2 years ago. The distension was slowly progressive without symptoms of neither digestive occlusion nor thoracic compression. Medical examination found important abdominal distension and a huge solid mass, fixed to the deep plan and occupying all abdominal cavity. Abdominal tomography revealed a giant mass measuring 30x22x26 cm. It had regular contours without capsular invasion and had multiple septa enhanced by contrast. It encased the right kidney and pressed back abdominal organs (Figure 1). This mass was in contact with the abdominal aorta and inferior vena cava without invasion of separation borders. This was an indicator of a very probable liposarcoma. Intraoperative data showed an encapsulated mass, adherent to inferior liver surface, and came back in contact with pancreas and large blood vessels (Figure 2). She underwent a surgical resection of the mass and the right kidney. The macroscopic examination showed a lobular tumor weighting 12 kg and measuring 50x40x18cm. It encased the kidney. Microscopic findings revealed a well differentiated liposarcoma features, totally removed without renal infiltration. Postoperative follow up was simple. She underwent a regular follow up by medical examination and CT scan, no recurrent tumor was found after 2 years.

Discussion

Liposarcoma is a rare mesenchymal tumor, it is frequently located in soft tissue of extremities and in 12 to 40 % in retroperitonium [3-5]. It affects equally men and women during the sixth and seventh decades of life [2]. Clinically, symptoms related to this affection are those of intra-abdominal mass such as abdominal pain, distension and constipation. Because of the deep localization, the tumor is often diagnosed at the advanced stage [6].

Histologically, Liposarcomas are divided to 5 subtypes, related to their cell predominance: Well-Differentiated Liposarcoma (WDL); Dedifferentiated Liposarcoma; Mixoid Liposarcoma; Pleomorphic liposarcoma and Spindle Cell Liposarcoma [1].

Computed tomography (CT) with contrast-enhancing and Magnetic resonance imaging (MRI) can show this tumor as fat density mass, streaky or mottled zones can be present. The localization and contact with intra-abdominal organs should be analyzed [1,3].

Complete surgical resection is the gold standard of treatment; it may include some organs, depending on the intraoperative findings such as kidney, spleen and pancreas… [7]. It can be limited in case of: vessel invasion, spinal cord and visceral invasion exceeding the possibilities of an enlarged resection [3,7].

Prognostic depends on degree of differentiation and quality of surgical resection. Local recurrence occurs often 2 up to 5 years after surgery [3].

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© 2018 Yazal SEL, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.