{"title":"Pediatric dermatology: internal and external medicine.","authors":"L M Solomon","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76171,"journal":{"name":"Modern problems in paediatrics","volume":"20 ","pages":"1-6"},"PeriodicalIF":0.0,"publicationDate":"1976-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12213056","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Toxic epidermal necrolysis - a review.","authors":"J M Beare","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76171,"journal":{"name":"Modern problems in paediatrics","volume":"20 ","pages":"118-26"},"PeriodicalIF":0.0,"publicationDate":"1976-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12213057","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The study of 198 collodion babies, 29 personal cases and 169 from the literature was undertaken. The collodion membrane with spontaneously desquamate between the 15th day and 3rd month of life. During the neonatal period one third of the infants die due to pulmonary complications or infection. The collodion membrane seems to have an increased permeability. The desquamation is followed by a relapse which leads to different keratinization disorders, most frequently nonbullous congenital ichthyosiform erythroderma.
{"title":"Collodion baby.","authors":"M Larregue, J M Bressieux, J P Fournet","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The study of 198 collodion babies, 29 personal cases and 169 from the literature was undertaken. The collodion membrane with spontaneously desquamate between the 15th day and 3rd month of life. During the neonatal period one third of the infants die due to pulmonary complications or infection. The collodion membrane seems to have an increased permeability. The desquamation is followed by a relapse which leads to different keratinization disorders, most frequently nonbullous congenital ichthyosiform erythroderma.</p>","PeriodicalId":76171,"journal":{"name":"Modern problems in paediatrics","volume":"20 ","pages":"40-9"},"PeriodicalIF":0.0,"publicationDate":"1976-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12212874","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Disseminate pigmented nevi and short stature.","authors":"L M Solomon, S Pruzansky","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76171,"journal":{"name":"Modern problems in paediatrics","volume":"20 ","pages":"165-6"},"PeriodicalIF":0.0,"publicationDate":"1976-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12212879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The organoid nevus is a malformation of most of the normal tissue components in a strictly localized, smaller or larger area of skin, most commonly the scalp. It undergoes more or less predictable developmental changes in puberty and then remains stable, but is subject to secondary development of benign or semimalignant adnexal tumors in a significant percentage of cases. It may present clinically and histologically in a variety of forms, the most common ones being nevus sebaceus and nevus verrucosus. It may be associated with neurologic and skeletal abnormalities in the organoid nevus syndrome (Schimmelpenning-Feuerstein-Mims). Total excision before adolescence is the treatment of choice.
{"title":"Organoid nevus.","authors":"H Pinkus","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The organoid nevus is a malformation of most of the normal tissue components in a strictly localized, smaller or larger area of skin, most commonly the scalp. It undergoes more or less predictable developmental changes in puberty and then remains stable, but is subject to secondary development of benign or semimalignant adnexal tumors in a significant percentage of cases. It may present clinically and histologically in a variety of forms, the most common ones being nevus sebaceus and nevus verrucosus. It may be associated with neurologic and skeletal abnormalities in the organoid nevus syndrome (Schimmelpenning-Feuerstein-Mims). Total excision before adolescence is the treatment of choice.</p>","PeriodicalId":76171,"journal":{"name":"Modern problems in paediatrics","volume":"20 ","pages":"50-7"},"PeriodicalIF":0.0,"publicationDate":"1976-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12212889","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Mutilating keratoderma (Vohwinkel).","authors":"J H Herndon, R G Freeman","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76171,"journal":{"name":"Modern problems in paediatrics","volume":"20 ","pages":"151-2"},"PeriodicalIF":0.0,"publicationDate":"1976-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11366450","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In 3 cases of lymphomatoid papulosis with few ulceronecrotic lesions and 5 with the classic features of pytiriasis lichenoides acuta with necrotic lesions, a considerable part of the cellular component of the infiltrate of the lesions showed the morphologic and cytochemical characteristics of the cells described as immunoblasts. The authors consider that the lymphomatoid papulosis could represent an immunoblastic response to an unknown antigen.
{"title":"Lymphomatoid papulosis. A model of immunoblastic reaction of the skin.","authors":"J Piñol-Aguadé, C Ferrándiz","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>In 3 cases of lymphomatoid papulosis with few ulceronecrotic lesions and 5 with the classic features of pytiriasis lichenoides acuta with necrotic lesions, a considerable part of the cellular component of the infiltrate of the lesions showed the morphologic and cytochemical characteristics of the cells described as immunoblasts. The authors consider that the lymphomatoid papulosis could represent an immunoblastic response to an unknown antigen.</p>","PeriodicalId":76171,"journal":{"name":"Modern problems in paediatrics","volume":"20 ","pages":"169-79"},"PeriodicalIF":0.0,"publicationDate":"1976-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12212877","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Leprosy in children is more frequent than generally thought. Diagnosis is not easily made because early signs of the diseases are overlooked. Statistic data from the Dermatologic Clinic Pascua of Mexico City reveal that early signs are cutaneous in 67% of cases: hypochromic and anesthetic infiltration, nodules, and alopecia of eyebrows and eyelashes. Neurological symptoms such as anesthesis, facial paralysis, thickening of nerves and trophic problems are present in 19.3% of cases. The nose mucosae are congested in 9.2% of cases. Systemic manifestations may be present in 4% of cases. Examination of contacts living with lepromatous patients is stressed as the best way to discover the early signs of the disease. Dermatological consultation in general and pediatric hospitals is also recommended. If diagnosis is delayed, leprosy can induce physical, psychological and social disabilitation of the patient.
{"title":"Early signs of leprosy in children.","authors":"A Saúl","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Leprosy in children is more frequent than generally thought. Diagnosis is not easily made because early signs of the diseases are overlooked. Statistic data from the Dermatologic Clinic Pascua of Mexico City reveal that early signs are cutaneous in 67% of cases: hypochromic and anesthetic infiltration, nodules, and alopecia of eyebrows and eyelashes. Neurological symptoms such as anesthesis, facial paralysis, thickening of nerves and trophic problems are present in 19.3% of cases. The nose mucosae are congested in 9.2% of cases. Systemic manifestations may be present in 4% of cases. Examination of contacts living with lepromatous patients is stressed as the best way to discover the early signs of the disease. Dermatological consultation in general and pediatric hospitals is also recommended. If diagnosis is delayed, leprosy can induce physical, psychological and social disabilitation of the patient.</p>","PeriodicalId":76171,"journal":{"name":"Modern problems in paediatrics","volume":"20 ","pages":"142-50"},"PeriodicalIF":0.0,"publicationDate":"1976-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12213058","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Progeria in childhood with description of a new progeroid syndrome displaying gross Fabry-like changes in heart, great vessels and kidneys.","authors":"E J Moynahan","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76171,"journal":{"name":"Modern problems in paediatrics","volume":"20 ","pages":"14-7"},"PeriodicalIF":0.0,"publicationDate":"1976-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12212870","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}