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O Tincopa Wong

Publications and source records attributed to O Tincopa Wong.

4 recordsLinked to original sources

[Vascular nevus. A study of its frequency, types and course].

It is presented a prospective study of vascular nevus during a year, with the finality to know its frequency, types and evolution. In twelve months of study, we founded in 1,485 borns that 14.14% presented those lesiones salmon stain 86%, oport wine 1.35%, capilar hemangioma or in strawberry the 10.81%, cavernous hemangioma the 0.45% and mixed hemangioma the 1.35%. Where more frequent in females that in males as well as from the urban zone in almost more than the half of the cases. Dimensions were between 0 to 5 cm. range, 98% in salmon stain, 95% in strawberry hemangioma, 66.3% mixed hemangioma, 66.6% in oport wine stain distributed in the head in more proportion. There was salmon stain in the nape in 61.7%, 15% in the forehead and in the superior eyelids 14.3%. The familiar antecedents of vascular nevus in brothers was of 4.76%, 5.71% in uncle, 2.98% in parents and 1.43% in grandparents. The evolution was not concluded because of desertion in almost the totality of patients, finalizing with only the 6.66%. Our findings are different from those published in the literature. The total frequency is more in our experience in salmon, oport wine stains and hemangiomas.

Female↗

[Congenital hemihypertrophy].

A case of congenital hemihypertrophy, which affects the right part hemi-tongue and the homolateral superior member, is reported in a just born of feminine sex, this patient has been observed until the age of one year and five months, at this age she was not controlled any more. Then the clinic history is reviewed and the clinic, associate congenital defects, are commented, also the existence of embryonal tumours, possible etiopathogenic hypothesis, treatment and prognostic.

Abnormalities, Multiple↗

[Aplasia cutis congenita. Report of 2 cases].

In 1983, we had two cases of pediatric patients, which were observed in the Regional Hospital "Victor Lazarte Echegaray" of the Peruvian Institute of Social Security in Trujillo, these cases correspond to the syndrome of aplasia cutis congenita. In the first case, the defect was localized as a of ulcer in the right inferior member, which was affected from the third part distal of the thigh to the back part of the foot. In the second one, the lesion was in the middle line of the hairy skin, and it had the particularity of being associate to others congenital malformations. These cases are mentioned because of their rarity of presentation at a world level as well as their unknown occurrence in our country. Then we comment the clinic, histological characteristics, associate congenital defects, possible etiopathogenic mechanisms, differential diagnostic and its evolution and treatment.

Abnormalities, Multiple↗

[Malignant acanthosis nigricans. Presentation of a case and a study of its incidence].

In the Regional Hospital "Victor Lazarte Echegaray" of Trujillo, Perú, it was made a study in order to determine the frequency of the acanthosis nigricans, associate to cancer (malignant acanthosis nigricans), during january 1978 to october 1983, and a case was founded in a patient of 62 years old, who had advanced adenocarcinoma gastric of one year and a half of evolution. The dermatosis was manifested with the neoplasia, which corresponds to a generalized form, with hyperkeratosis palmo plantar, with whole loss of the axillary hair and only part of the pubic region, the mucous membranes were not affected. The patient survived 3 months after the diagnostic were made.

Acanthosis Nigricans↗