6 research outputs found
Angiokeratoma circumscriptum naeviforme with soft tissue hypertrophy and deep venous malformation: A variant of Klippel-Trenaunay syndrome?
Klippel-Trenaunay syndrome (KTS) is a cutaneous capillary malformation on a limb in association with soft tissue swelling with or without bony hypertrophy and atypical varicosity. The capillary malformation associated with KTS is port wine stain. Angiokeratoma circumscriptum naeviforme (ACN) is a congenital variant of angiokeratoma commonly present on the lower limb as a hyperkeratotic plaque. ACN is rarely associated with KTS. We report a case of ACN with soft tissue hypertrophy and deep venous malformation (possibly a variant of Klippel-Trenaunay) in a 4-year-old male child
Rare case of giant chorioangioma and review of literature
Placental tumours are classified into trophoblastic and nontrophoblastic tumours. Nontrphoblastic tumours are relatively rare which includes chorioangioma/placental hemangioma, placental teratoma, placental metastatis. Chorioangioma has a prevalence of 1% among other placental tumours. Giant chorioangioma is relatively rare. Chorioangioma may be associated with adverse fetal and maternal complications. Fetal complications may include intrauterine fetal growth retardation, fetal anemia, polyhydramnios and maternal complications may include pregnancy induced hypertension, antepartum hemorrhage, preterm labour. Untoward complications can be avoided by timely detection, appropriate follow up and management. We report a case of giant chorioangioma and its outcome
Communicating Tubular Duplication of Upper Esophagus–A Rare Occurrence
Duplications of esophagus are commonly classified into two types, tubular and cystic. Tubular duplication of esophagus is a rare occurrence and is much less common than cystic duplication of foregut. Most esophageal duplications are located in the lower third of the esophagus. A cervical esophageal duplication is extremely rare. Esophageal duplications have been reported twice as commonly on the right as on the left. We report a case of incidental finding identified on computed tomography of communicating tubular esophageal duplication involving the left side of the upper esophagus in a tuberculosis patient that was subsequently confirmed on barium swallow test