Cystic Lymphangioma of the Rectus Abdominis Muscle: An Extremely Rare Clinical Entity

Saloua Ammar; Mohamed Jallouli*; Mahdi Ben Dhaou; Riadh Mhiri Department of Pediatric Surgery, Hedi Chaker Hospital, School of Medicine, Sfax University, Sfax, Tunisia Received: Dec 11, 2013; Accepted: Jul 10, 2014; First Online Available: Jul 19, 2014 Cystic lymphangioma is a rare malformative benign tumor of the lymphatic vessels. It occurs most commonly in the neck. Rarely they are known to involve the axilla, groin, mediastinum, retroperitoneum, pelvis, mesentery, omentum and spleen[1]. A 10 year old girl, without any particular pathological history, presented with complaints of swelling in the left side of abdomen increasing very slowly in size since the age of 3 years. Physical examination objectified left parietal bulk, compressible, by 5 cm long axis without signs of acute inflammation. Abdominal US showed a left paramedian parietal mass sub umbilical developed at the expense of the rectus abdominis muscle. This mass was well limited, measuring 57×41 mm, hypoechoic, micro cystic with many thin septa. She arrived deeply in contact with bowel loops and iliac vessels. Further exploration by MRI showed a polylobed mass, developed at the expense of the rectus abdominis muscle. It extended to the large muscles of the ipsilateral side, with a hypo-signal T1 and hyper-signal T2. This formation was responsible for ascension of small bowel and came in contact with the external iliac pedicle, the left psoas muscle and the sigmoid without invasion. The MRI appearance was compatible with a cystic lymphangioma. Per operatively, the cystic mass was attached at the rectus abdominis muscle (Fig. 1). Entire dissection and excision of the mass sacrificing a musculofacia piece and a tab of the parietal peritoneum were performed. There was no adhesion with the iliac vessels. Histological examination revealed an intramuscular cystic lymphangioma extending to the peritoneum. The postoperative course was uneventful. Subsequent control after 10 months showed a child in remission. Fig. 1: Abdominal MRI: hypersignal mass developed at the expense of the rectus abdominis with a contact with the psoas muscle, the sigmoid colon and the external iliac pedicle Cystic lymphangioma is a rare congenital malformation. The failure of connection or separation between the lymphatic and venous system and the proliferation of abnormal lymphatic tissue are two theories most implicated in its development[2]. Most of the cystic lymphangiomas are discovered during childhood; however, their nascent presentation in adults is also reported[3]. It can manifest anywhere in the body. The common locations are cervico-facial regions. Muscle location, extremely scarse, was described both in adults[3] and children[4] but not in the rectus abdominis muscle. The clinical presentation of cystic lymphangioma is polymorphic, unspecific and variable depending on the location and extent. In front of a cystic mass localized in the muscle several diagnostics can be evoked, such as hematoma or cystic muscle remodeling especially following trauma or tumor lesions or muscle abscess[3]. Imaging in our case was highly suggestive of the diagnosis. US[5] and MRI[3,5,6] are excellent ways for diagnosis of cystic lymphangiomas in several locations. US usually shows multicystic lesion with internal septations and no blood flow is detected on color doppler ultrasonographs. Other modalities like CT scan and MRI can be employed to delineate the lesion, in a better way. A CT scan demonstrates multicystic, homogeneous, non-invasive density with low attenuation. These modalities are usually helpful in ascertaining the extent of the lesion and