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Intraabdominal lymphangiomyoma in an infant with protein-losing

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dc.contributor.author Koltuksuz, U
dc.contributor.author Ozgen, U
dc.contributor.author Ozen, S
dc.contributor.author Sarac, K
dc.contributor.author Gursoy, MH
dc.date.accessioned 2022-03-07T12:50:09Z
dc.date.available 2022-03-07T12:50:09Z
dc.date.issued 2000
dc.identifier.uri http://hdl.handle.net/11616/54525
dc.description.abstract Lymphangiomyoma is an extremely rare tumor occurring exclusively in women of reproductive age. The tumor is characterized by proliferation of immature smooth muscle along the lymphatic vessels of the abdomen, thorax and lung. Although lymphangiomyoma has been reported in a young girl and a girl infant, none has been reported in boys. We report herein a case of lympangiomyoma in a two-year-old boy. The unusual presentation in this patient was that the tumor arose from the small bowel mesentery without any evidence of lung involvement. The tumor was extirpated and lymphangiomyomatosis was confirmed pathologically.
dc.source TURKISH JOURNAL OF PEDIATRICS
dc.title Intraabdominal lymphangiomyoma in an infant with protein-losing
dc.title enteropathy and hemihypertrophy


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