Results 1 to 10 of about 7,643 (212)

Isolated mediastinal lymphangioma in a child: A rare case report [PDF]

open access: yesSouth African Journal of Radiology
The mediastinum is an unusual location for cystic lymphangiomas. An 18-month-old male presented with acute fever, dry intermittent cough and respiratory distress.
Ankita Gupta   +4 more
doaj   +2 more sources

Correlative imaging of cystic lymphangiomas: ultrasound, CT and MRI comparison [PDF]

open access: yesActa Radiologica Open, 2015
Background Cystic lymphangioma is a rare benign lesion derived from the detachment of the lymph sacs from venous drainage systems; the treatment of choice is a surgical excision and the final diagnosis is of histological type.
Valeria Romeo   +6 more
doaj   +3 more sources

Endoscopy-assisted surgical management for a giant axillary cystic lymphangioma: a case report [PDF]

open access: yesFrontiers in Surgery
A cystic lymphangioma is a benign malformation that arises from aberrant lymphatic development and commonly occurs in the neck and axilla. While typically asymptomatic, complete surgical excision remains the primary treatment.
Hai-wei Chen   +3 more
doaj   +2 more sources

Cystic Lymphangioma of Rectum-A Case Report and Review of Literature

open access: yesThe Korean Journal of Gastroenterology, 2023
Colorectal cystic lymphangiomas are rare benign lesions. They are characterized by the presence of either single or multi-cystic spaces lined by endothelium. Though there are multiple case reports of right and transverse colonic lymphangioma; only around
Govindraj S Dessai   +4 more
doaj   +1 more source

Mesenteric cystic lymphangioma mimicking an ileo-colic intussusception

open access: yesJournal of Pediatric Surgery Case Reports, 2020
Lymphangioma accounts for 5% of benign pediatric tumors and less than 1% is located in the abdomen. Indeed mesenteric cystic lymphangioma is a rare benign abdominal mass and its pathogenesis is still unknown.Mesenteric cystic lymphangioma is often ...
Elisa Mina   +7 more
doaj   +1 more source

Cystic Lymphangioma of Pancreas [PDF]

open access: yesIndian Journal of Surgical Oncology, 2015
Lymphangiomas are benign hamartomatous malformations which can arise either from congenitally sequestered lymphatic channels or due to acquired obstruction caused by fibrosis of lymph channels. They are common in the pediatric age group in the soft tissue of neck and the axilla. Abdominal lymphangiomas are rare; even rarer is the primary involvement of
Chhagan, Bihari   +5 more
openaire   +2 more sources

Adrenal Cystic Lymphangioma [PDF]

open access: yesWest Indian Medical Journal, 2015
The Editor Sir, A previously healthy five-year old boy was evaluated for intermittent abdominal pain lasting for six months. Physical examination was normal but abdominal ultrasonography revealed a 3.5 × 4 cm lobulated cystic mass located in the right adrenal region.
O, Bosnalı   +2 more
openaire   +2 more sources

Acquired cystic lymphangioma imitating breast cancer recurrence

open access: yesRadiology Case Reports, 2023
Cystic lymphangioma is a benign, congenital lymphatic malformation mainly encountered in infants during the first 2 years of life. It is rarely found in adults.
Safaa Choayb, MD   +5 more
doaj   +1 more source

Retroperitoneal cystic lymphangioma [PDF]

open access: yesIndian Journal of Surgery, 2008
123 A 50-year-old man presented with vague abdominal discomfort and progressive abdominal swelling since 8 months. There was no history of previous medical and surgical problems including trauma. The only positive fi nding on physical examination was the presence of a large fi xed left sided abdominal mass.
Ali, Aminian   +5 more
openaire   +4 more sources

An adrenal cystic lymphangioma: A case report of a rare tumor

open access: yesUrology Case Reports, 2019
Cystic lymphangioma is a rare benign tumor developing from lymphatic endothelial cells, and is usually described in the neck or axilla. We report a new case of an adrenal cystic lymphangioma fortuitously found in a 37-year-old patient.
Selim Zaghbib   +5 more
doaj   +1 more source

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