Results 181 to 190 of about 11,533 (222)
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Urologia Internationalis, 2010
We report a case of urethral lymphangioma presenting with frank, painless hemaluria as the only symptom. Such a case has not been described in the literature to our knowledge.
N A, Jadeja, S P, Yadav
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We report a case of urethral lymphangioma presenting with frank, painless hemaluria as the only symptom. Such a case has not been described in the literature to our knowledge.
N A, Jadeja, S P, Yadav
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International Journal of Urology, 2002
AbstractLymphangiomas are rare benign tumors that are congenital malformations of the lymphatic system. Most cases present in children as a soft, cystic mass in the neck and the axilla. Primary renal lymphangioma is exceedingly rare, with only 35 cases reported so far. We report a case of primary lymphangioma arising from the kidney.
Ichiya, Honma +6 more
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AbstractLymphangiomas are rare benign tumors that are congenital malformations of the lymphatic system. Most cases present in children as a soft, cystic mass in the neck and the axilla. Primary renal lymphangioma is exceedingly rare, with only 35 cases reported so far. We report a case of primary lymphangioma arising from the kidney.
Ichiya, Honma +6 more
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British Journal of Oral and Maxillofacial Surgery, 1986
Lymphangiomas of the tongue are relatively uncommon developmental anomalies, which may present as either localised or diffuse lesions. Two cases are reported, and the literature reviewed.
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Lymphangiomas of the tongue are relatively uncommon developmental anomalies, which may present as either localised or diffuse lesions. Two cases are reported, and the literature reviewed.
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Pediatric Emergency Care, 1995
Lymphangiomas are uncommon congenital tumors of the lymphatic system which usually occur in the head and neck; involvement of the tongue is rare. We report the case of a six-year-old Asian girl with a lymphangioma of the tongue. The differential diagnosis and treatment of tongue lymphangioma are also reviewed.
B, Lobitz, T, Lang
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Lymphangiomas are uncommon congenital tumors of the lymphatic system which usually occur in the head and neck; involvement of the tongue is rare. We report the case of a six-year-old Asian girl with a lymphangioma of the tongue. The differential diagnosis and treatment of tongue lymphangioma are also reviewed.
B, Lobitz, T, Lang
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The Annals of Thoracic Surgery, 2008
We report on the very rare case of a 49-year-old man with a large solitary pulmonary lymphangioma. Rapid growth of the tumor led to dyspnea and pain. A chest roentgenogram and computed tomography scan revealed a large 18 x 12-cm space-occupying cystic lesion in the posterior mediastinum. The tumor was resected by lateral thoracotomy.
Stefan, Limmer +2 more
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We report on the very rare case of a 49-year-old man with a large solitary pulmonary lymphangioma. Rapid growth of the tumor led to dyspnea and pain. A chest roentgenogram and computed tomography scan revealed a large 18 x 12-cm space-occupying cystic lesion in the posterior mediastinum. The tumor was resected by lateral thoracotomy.
Stefan, Limmer +2 more
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The Indian Journal of Pediatrics, 2001
Thoracic lymphangioma is a benign congenital condition that may involve any organ within the chest. Here, a case of intra thoracic isolated extramediastinal lymphangioma is reported. The child had respiratory distress from neonatal period. Surgery completely cured the patient. However, it is only the 3rd reported case in English literature.
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Thoracic lymphangioma is a benign congenital condition that may involve any organ within the chest. Here, a case of intra thoracic isolated extramediastinal lymphangioma is reported. The child had respiratory distress from neonatal period. Surgery completely cured the patient. However, it is only the 3rd reported case in English literature.
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American Journal of Roentgenology, 2005
Ly JQ, Gilbert BC, Davis SW, Beall DP, Richardson RR 2-year-old girl who was known to have Turner’s syndrome presented to her primary care provider with an enlarging mass involving her left foot. Physical examination revealed that the left foot was diffusely enlarged but not discolored. Conventional radiography (Fig.
Justin Q, Ly +4 more
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Ly JQ, Gilbert BC, Davis SW, Beall DP, Richardson RR 2-year-old girl who was known to have Turner’s syndrome presented to her primary care provider with an enlarging mass involving her left foot. Physical examination revealed that the left foot was diffusely enlarged but not discolored. Conventional radiography (Fig.
Justin Q, Ly +4 more
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Acta Paediatrica, 1973
SummaryTwo operations upon a giant gluteal lymph‐angioma in a boy were complicated by massive haemorrhage. The complication proved to be due to fibrinolysis stimulated by activators released by the tumour. The diagnosis was confirmed by the demonstration of high fibrino‐lytic activity and FDP in blood and discharge drained from the wound.
R, Kornfält, I M, Nilsson, L, Okmian
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SummaryTwo operations upon a giant gluteal lymph‐angioma in a boy were complicated by massive haemorrhage. The complication proved to be due to fibrinolysis stimulated by activators released by the tumour. The diagnosis was confirmed by the demonstration of high fibrino‐lytic activity and FDP in blood and discharge drained from the wound.
R, Kornfält, I M, Nilsson, L, Okmian
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Gastrointestinal Radiology, 1976
Eleven cases of colonic lymphangioma, including 3 that have not been reported previously, are reviewed. Radiologic analysis reveals that 9 presented as polypoidal mucosal lesions and only 2 had characteristic features at a submucosal lesion. A predominant occurence in females (70%) and during the sixth and seventh decades are noted.
J P, Lawson, P J, Myerson, D A, Myerson
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Eleven cases of colonic lymphangioma, including 3 that have not been reported previously, are reviewed. Radiologic analysis reveals that 9 presented as polypoidal mucosal lesions and only 2 had characteristic features at a submucosal lesion. A predominant occurence in females (70%) and during the sixth and seventh decades are noted.
J P, Lawson, P J, Myerson, D A, Myerson
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Journal of Urology, 1983
We report the first case of a lymphangioma arising from the wall of the bladder, protruding into the lumen on 1 side and invading the peritoneal cavity on the other side. The presenting sign was painless macroscopic hematuria that had occurred initially 2 months before hospitalization. Treatment consisted of partial cystectomy.
M, Bolkier +3 more
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We report the first case of a lymphangioma arising from the wall of the bladder, protruding into the lumen on 1 side and invading the peritoneal cavity on the other side. The presenting sign was painless macroscopic hematuria that had occurred initially 2 months before hospitalization. Treatment consisted of partial cystectomy.
M, Bolkier +3 more
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