Cystic Lymphangioma

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James Mcdermott - One of the best experts on this subject based on the ideXlab platform.

Andrew Dries - One of the best experts on this subject based on the ideXlab platform.

Rebecca Burbridge - One of the best experts on this subject based on the ideXlab platform.

  • retroperitoneal Cystic Lymphangioma diagnosed by endoscopic ultrasound guided fine needle aspiration
    Clinical Endoscopy, 2013
    Co-Authors: Tyler P Black, Cynthia D Guy, Rebecca Burbridge
    Abstract:

    Retroperitoneal Cystic Lymphangiomas are rare tumors of the lymphatic system. These tumors usually present in childhood and are often diagnosed incidentally with imaging procedures. Although benign, they can grow to large sizes and become symptomatic due to their compressive effects. They can cause diagnostic dilemmas with other retroperitoneal Cystic tumors including those arising from the liver, kidney, and pancreas. Endoscopic ultrasound (EUS) has become an invaluable tool in the assessment of Cystic lesions in the region of the pancreas. This case describes a 66-year-old female who presented with 3 months of abdominal pain. Radiographic imaging was suggestive of a Cystic lesion in the region of the pancreas. EUS was performed confirming a Cystic lesion adjacent to the tail of the pancreas with subsequent fine needle aspiration fluid analysis consistent with a Cystic Lymphangioma.

Zoubeir Ben Safta - One of the best experts on this subject based on the ideXlab platform.

  • surgical management of intra abdominal Cystic Lymphangioma report of 20 cases
    World Journal of Surgery, 2012
    Co-Authors: Amin Makni, F Chebbi, Fadhel Fetirich, R Ksantini, H Bedioui, M Jouini, Montassar Kacem, Zoubeir Ben Safta
    Abstract:

    Background Cystic Lymphangioma (CL) is a benign rare malformation of lymphatic vessels. Its discovery in adults is rare. Although it can affect any organ, the common forms found in adults are mesenteric and/or retroperitoneal CL. This article was designed to study the epidemiological, diagnostic difficulties, and therapeutic principles of intra-abdominal Cystic Lymphangioma in adults.

  • surgical management of intra abdominal Cystic Lymphangioma report of 20 cases
    World Journal of Surgery, 2012
    Co-Authors: Amin Makni, F Chebbi, Fadhel Fetirich, R Ksantini, H Bedioui, M Jouini, Montassar Kacem, Zoubeir Ben Safta
    Abstract:

    Cystic Lymphangioma (CL) is a benign rare malformation of lymphatic vessels. Its discovery in adults is rare. Although it can affect any organ, the common forms found in adults are mesenteric and/or retroperitoneal CL. This article was designed to study the epidemiological, diagnostic difficulties, and therapeutic principles of intra-abdominal Cystic Lymphangioma in adults. We report a retrospective study from January 1998 to September 2010 concerning 20 patients who underwent surgical removal of a CL. We were interested in discovering the clinical, biological, and radiological characteristics of CL. The localization, size, and number of cysts have been reported, as well as the surgical intervention used and the postoperative immediate and late complications. The median age was 46 years. Abdominal pain was the main symptom and was found in 15 patients (75%). Physical examination revealed an abdominal mass in 12 patients (60%). In four patients (20%), the Cystic Lymphangioma was incidental. Abdominal ultrasound and abdominal CT scan helped to highlight 22 Cystic masses. CL diagnosis was established preoperatively in 13 patients (65%). Six patients (30%) were operated with a diagnosis other than CL. The diagnosis was made intraoperatively in one case (5%). Only two patients (10%) were operated on in emergency: one due to an infected CL and the other was CL complicated with intraCystic hemorrhage. A laparotomy in 13 cases (65%) was the surgical approach used, whereas 7 cases (35%) benefited from a laparoscopy. No conversion was noted. The majority of the patients, 18 cases (90%), received a total cystectomy. Only two patients (10%) had recurrences of which only one was reoperated. The diagnosis of CL often is facilitated by means of modern imaging; however, other diagnoses may be discussed, particularly hydatid disease endemic areas. If symptomatic lesions or complications arise, complete surgical excision, when possible without major sacrifice, seems to be the best therapeutic option to reduce the risk of recurrence.

Tyler P Black - One of the best experts on this subject based on the ideXlab platform.

  • retroperitoneal Cystic Lymphangioma diagnosed by endoscopic ultrasound guided fine needle aspiration
    Clinical Endoscopy, 2013
    Co-Authors: Tyler P Black, Cynthia D Guy, Rebecca Burbridge
    Abstract:

    Retroperitoneal Cystic Lymphangiomas are rare tumors of the lymphatic system. These tumors usually present in childhood and are often diagnosed incidentally with imaging procedures. Although benign, they can grow to large sizes and become symptomatic due to their compressive effects. They can cause diagnostic dilemmas with other retroperitoneal Cystic tumors including those arising from the liver, kidney, and pancreas. Endoscopic ultrasound (EUS) has become an invaluable tool in the assessment of Cystic lesions in the region of the pancreas. This case describes a 66-year-old female who presented with 3 months of abdominal pain. Radiographic imaging was suggestive of a Cystic lesion in the region of the pancreas. EUS was performed confirming a Cystic lesion adjacent to the tail of the pancreas with subsequent fine needle aspiration fluid analysis consistent with a Cystic Lymphangioma.