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2.
Cir Cir ; 84(6): 509-512, 2016.
Article in Spanish | MEDLINE | ID: mdl-26688477

ABSTRACT

BACKGROUND: Mesenteric lymphangioma are rare tumours. They usually present early on in life, if congenital, or soon after trauma. The usual sites of presentation of lymphangiomas are in the neck, and axillae. In the abdomen they are more common in the mesentery, primarily of the ileum, or retroperitoneal. OBJECTIVE: A rare case is presented of a mesenteric lymphangioma. CLINICAL CASE: It involves an elderly African-American male, many years after trauma, and characterised with early satiety, causing weight loss, but without gastric outlet obstruction or vomiting. Its diagnosis, management and review of literature are presented. CONCLUSIONS: Mesenteric cysts are rare tumours that should be included as differential diagnosis in elderly patients with a history of previous abdominal trauma.


Subject(s)
Lymphangioma, Cystic/etiology , Omentum/pathology , Peritoneal Neoplasms/etiology , Aged , Diagnosis, Differential , Humans , Laparotomy , Liver/injuries , Lymphangioma, Cystic/congenital , Lymphangioma, Cystic/pathology , Lymphangioma, Cystic/surgery , Magnetic Resonance Imaging , Male , Nausea/etiology , Omentum/surgery , Peritoneal Neoplasms/congenital , Peritoneal Neoplasms/pathology , Peritoneal Neoplasms/surgery , Reoperation , Satiation , Time Factors , Tissue Adhesions/surgery , Tomography, X-Ray Computed , Wounds, Gunshot
3.
Eksp Klin Gastroenterol ; (1): 84-7, 2015.
Article in Russian | MEDLINE | ID: mdl-26281166

ABSTRACT

Congenital chylous ascites is a rare polietiologic entity, requiring close study of the infant's organism by visualization methods in order to diagnose the bening or malignant underlying pathology. In the article is given a report on case of congenital chylous ascites in infant, caused by lymphangioma in the peritoneal cavity. Atypical clinic and the lack of diagnostic standards led to the later detection of the ascite's origin.


Subject(s)
Chylous Ascites/congenital , Chylous Ascites/pathology , Lymphangioma/congenital , Lymphangioma/pathology , Peritoneal Neoplasms/congenital , Peritoneal Neoplasms/pathology , Humans , Infant , Male
8.
South Med J ; 85(2): 201-3, 1992 Feb.
Article in English | MEDLINE | ID: mdl-1738891

ABSTRACT

Gastrointestinal hemangiomas, though rare, can be an important source of GI bleeding in infants. In the past, diagnosis has been hampered by a lack of reliable methods. With the recent advent of selective mesenteric angiography, the suspected diagnosis can be readily confirmed. Surgical resection remains the definitive therapy; steroid therapy has produced conflicting results.


Subject(s)
Anemia/etiology , Hemangioma/complications , Ileal Neoplasms/complications , Ileocecal Valve , Mesentery , Peritoneal Neoplasms/complications , Anemia/diagnosis , Chronic Disease , Female , Head and Neck Neoplasms/congenital , Hemangioma/congenital , Hemangioma/diagnosis , Humans , Ileal Neoplasms/congenital , Ileal Neoplasms/diagnosis , Infant , Melena/diagnosis , Melena/etiology , Peritoneal Neoplasms/congenital , Peritoneal Neoplasms/diagnosis , Skin Neoplasms/congenital
9.
Zentralbl Allg Pathol ; 135(7): 685-8, 1989.
Article in English | MEDLINE | ID: mdl-2588834

ABSTRACT

A case of a female fetus born with multiple developmental defects and leiomyomatosis peritonealis disseminata (LPD) is reported. The authors suspect that similar etiologic factors may be responsible for both the developmental defects and LPD.


Subject(s)
Abnormalities, Multiple , Leiomyoma/congenital , Peritoneal Neoplasms/congenital , Female , Humans , Infant, Newborn , Leiomyoma/pathology , Peritoneal Neoplasms/pathology
10.
Eur J Pediatr ; 147(4): 428-30, 1988 May.
Article in English | MEDLINE | ID: mdl-3294016

ABSTRACT

Malignant mesothelioma was diagnosed in a 16-day-old boy. As far as we know this is the first report of a congenital case of this disease.


Subject(s)
Mesothelioma/congenital , Peritoneal Neoplasms/congenital , Cytoplasm/ultrastructure , Humans , Infant, Newborn , Male , Mesothelioma/secondary , Mesothelioma/ultrastructure , Microscopy, Electron , Neoplasm Metastasis , Peritoneal Neoplasms/ultrastructure
12.
J Pediatr Surg ; 18(3): 243-5, 1983 Jun.
Article in English | MEDLINE | ID: mdl-6875770

ABSTRACT

Only three primary peritoneal mesotheliomas in children have been previously reported. We describe a 6-wk-old girl with a papillary peritoneal mesothelioma of low grade malignancy. This is probably a congenital mesothelioma and is the youngest patient reported to date.


Subject(s)
Mesothelioma/congenital , Peritoneal Neoplasms/congenital , Female , Humans , Infant , Mesothelioma/pathology , Peritoneal Neoplasms/pathology
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