Results 121 to 130 of about 20,169 (163)
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Dermatology, 2001
A case of Proteus syndrome is presented, in which severe hemihypertrophy of the left trunk and left lower extremity, scoliosis, endometriosis and huge bizarre-shaped body tumors were observed. Up to 22.6 kg of tumorous tissue was excised. This syndrome was first described in 1983.
H, Yasuda +5 more
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A case of Proteus syndrome is presented, in which severe hemihypertrophy of the left trunk and left lower extremity, scoliosis, endometriosis and huge bizarre-shaped body tumors were observed. Up to 22.6 kg of tumorous tissue was excised. This syndrome was first described in 1983.
H, Yasuda +5 more
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Pediatric Dermatology, 1994
Abstract: A 10‐month‐old girl had macrodactyly, facial and extremity hemihypertrophy, plantar cerebriform hyperpiasia, a subcutaneous mass on the back, macrocephaly, and lumbar kyphosis. These findings were diagnostic of Proteus syndrome. The clinical features, etiology, management, and points of differential diagnosis are discussed.
G L, Darmstadt, A T, Lane
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Abstract: A 10‐month‐old girl had macrodactyly, facial and extremity hemihypertrophy, plantar cerebriform hyperpiasia, a subcutaneous mass on the back, macrocephaly, and lumbar kyphosis. These findings were diagnostic of Proteus syndrome. The clinical features, etiology, management, and points of differential diagnosis are discussed.
G L, Darmstadt, A T, Lane
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Dermatology, 2009
Proteus syndrome is a rare hamartomatous syndrome with a variety of abnormalities. A 6-year-old Japanese boy without apparent abnormalities at birth developed by 1 year of age cerebriform skin tumors on the right sole, soft masses on the left sole, palms and fingers, brownish verrucous lesions and whorled brownish patches on the right side of the neck,
K, Sayama +4 more
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Proteus syndrome is a rare hamartomatous syndrome with a variety of abnormalities. A 6-year-old Japanese boy without apparent abnormalities at birth developed by 1 year of age cerebriform skin tumors on the right sole, soft masses on the left sole, palms and fingers, brownish verrucous lesions and whorled brownish patches on the right side of the neck,
K, Sayama +4 more
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Pediatric Dermatology, 1989
The term Proteus syndrome was coined in 1983 to describe a disorder of skeletal, hamartomatous, and other mesodermal malformations. The syndrome was named after the Greek god Proteus, whose name means "the Polymorphous." Clinical features of this new syndrome are currently being defined.
T, Costa, B R, Krafchik
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The term Proteus syndrome was coined in 1983 to describe a disorder of skeletal, hamartomatous, and other mesodermal malformations. The syndrome was named after the Greek god Proteus, whose name means "the Polymorphous." Clinical features of this new syndrome are currently being defined.
T, Costa, B R, Krafchik
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International Journal of Dermatology, 2000
A 7‐year‐old girl presented with a history of wine‐colored tumoral lesions on her leg, right foot, abdomen, and back, present since birth. They bled easily on touch or on minimal trauma. Soft, skin‐colored tumors were also present on the pectoral and left axillary regions. All the lesions had increased in size gradually.
J A, Cavero, E G, Castro, L, Junco
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A 7‐year‐old girl presented with a history of wine‐colored tumoral lesions on her leg, right foot, abdomen, and back, present since birth. They bled easily on touch or on minimal trauma. Soft, skin‐colored tumors were also present on the pectoral and left axillary regions. All the lesions had increased in size gradually.
J A, Cavero, E G, Castro, L, Junco
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Vasa, 2003
A 34-year-old male patient was referred with a recalcitrant leg ulcer overlying an extensive vascular malformation, which had led several times to septic soft tissue infections. During his infancy he had been diagnosed to have Klippel-Trenaunay syndrome.
G, Dragieva +6 more
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A 34-year-old male patient was referred with a recalcitrant leg ulcer overlying an extensive vascular malformation, which had led several times to septic soft tissue infections. During his infancy he had been diagnosed to have Klippel-Trenaunay syndrome.
G, Dragieva +6 more
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Journal of Paediatrics and Child Health, 1997
Abstract: This female Asian (Malay) baby had clinical features of Proteus syndrome. She had a large right facial lipolymphangioma with hyperpigmentation of the overlying skin. There was a smaller lymphangioma over the left side of her neck with excess nuchal folds, macrodactyly and bilateral talipes equinovarus.
S C, Ng, B S, Khoo, N K, Ho
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Abstract: This female Asian (Malay) baby had clinical features of Proteus syndrome. She had a large right facial lipolymphangioma with hyperpigmentation of the overlying skin. There was a smaller lymphangioma over the left side of her neck with excess nuchal folds, macrodactyly and bilateral talipes equinovarus.
S C, Ng, B S, Khoo, N K, Ho
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Macrodactyly in Proteus Syndrome
Journal of Hand Surgery, 1993A case of Proteus syndrome in a 13-year-old boy with macrodactyly, hemihypertrophy, exostosis of the skull, epidermal naevi, palmar and plantar masses, and scoliosis is reported. Macrodactyly involving the left thumb was treated surgically. The usual findings in macrodactyly, hypertrophy of the digital nerves and proliferation of subcutaneous fat, were
H, Miura +3 more
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American Journal of Medical Genetics, 1995
AbstractWe report on 2 children with Proteus syndrome who developed neoplasms. Patient 1 had a probable mesothelioma, although papillary carcinoma of the thyroid could not be completely ruled out. Patient 2 had bilateral ovarian serous cystadenomas with nuclear atypia.
P L, Gordon +3 more
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AbstractWe report on 2 children with Proteus syndrome who developed neoplasms. Patient 1 had a probable mesothelioma, although papillary carcinoma of the thyroid could not be completely ruled out. Patient 2 had bilateral ovarian serous cystadenomas with nuclear atypia.
P L, Gordon +3 more
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Annals of Plastic Surgery, 2002
Proteus syndrome is a very rare congenital condition comprising malformations and overgrowth of multiple sorts of tissue. It was described for the first time in 1979 and was termed Proteus syndrome in 1983. The authors describe a 37-year-old patient who was diagnosed initially as having Klippel-Trenaunay-Weber syndrome at the age of 10 years.
Edwin, Müller +2 more
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Proteus syndrome is a very rare congenital condition comprising malformations and overgrowth of multiple sorts of tissue. It was described for the first time in 1979 and was termed Proteus syndrome in 1983. The authors describe a 37-year-old patient who was diagnosed initially as having Klippel-Trenaunay-Weber syndrome at the age of 10 years.
Edwin, Müller +2 more
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