Results 181 to 190 of about 10,844 (225)
Some of the next articles are maybe not open access.
Pediatric Dermatology, 2007
Abstract: Lymphangiomas are congenital malformations of the lymphatic system. We report a 10‐year‐old boy with lymphatic malformation of the scrotum, which presented as a multiloculated scrotal mass associated with edema of the left thigh and left cryptorchidism. Histopathologic examination showed scrotal lymphangioma cavernosum.
Jelica, Vikicevic +4 more
openaire +2 more sources
Abstract: Lymphangiomas are congenital malformations of the lymphatic system. We report a 10‐year‐old boy with lymphatic malformation of the scrotum, which presented as a multiloculated scrotal mass associated with edema of the left thigh and left cryptorchidism. Histopathologic examination showed scrotal lymphangioma cavernosum.
Jelica, Vikicevic +4 more
openaire +2 more sources
Mayo Clinic Proceedings, 1986
Of 14 cases of intrathoracic lymphangioma, 4 occurred in the anterior, 5 in the superior, and 4 in the posterior mediastinum. One lesion was diffuse and associated with disappearing bone disease (Gorham's disease). The anterior mediastinal lymphangiomas occurred in adults and seemed to arise from the mediastinum.
L R, Brown +4 more
openaire +2 more sources
Of 14 cases of intrathoracic lymphangioma, 4 occurred in the anterior, 5 in the superior, and 4 in the posterior mediastinum. One lesion was diffuse and associated with disappearing bone disease (Gorham's disease). The anterior mediastinal lymphangiomas occurred in adults and seemed to arise from the mediastinum.
L R, Brown +4 more
openaire +2 more sources
Urologia Internationalis, 1998
We report a case of scrotal lymphangioma. A 6-year-old boy was referred to our hospital due to a right scrotal mass with tenderness. On physical examination the mass was discriminated from the testis and showed transillumination. Total surgical excision of the mass was performed. The lesion was multicystic, and adherent to the skin.
T, Yasui +3 more
openaire +2 more sources
We report a case of scrotal lymphangioma. A 6-year-old boy was referred to our hospital due to a right scrotal mass with tenderness. On physical examination the mass was discriminated from the testis and showed transillumination. Total surgical excision of the mass was performed. The lesion was multicystic, and adherent to the skin.
T, Yasui +3 more
openaire +2 more sources
Scottish Medical Journal, 1983
Lymphangioma of kidney is a rare, symptomatic but benign tumour. A case is reported and the literature reviewed. Aetiology and its effect on the incidence, non-invasive investigation, treatment and pathology are discussed.
D R, Singer, J D, Miller, G, Smith
openaire +2 more sources
Lymphangioma of kidney is a rare, symptomatic but benign tumour. A case is reported and the literature reviewed. Aetiology and its effect on the incidence, non-invasive investigation, treatment and pathology are discussed.
D R, Singer, J D, Miller, G, Smith
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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.
openaire +2 more sources
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.
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources