Apoorva Gupta, M. Bansal, S. Gulati, Vatsala Gupta, Vinod K. Sharma
Erythroderma or exfoliative dermatitis is characterized by erythema and scaling affecting more than 90% of the body surface area. Drug-induced erythrodermas are relatively uncommon in children but can be potentially life-threatening. We hereby report an unusual case of erythroderma due to oral intake of Giloy (Tinospora cordifolia) in a 10-year-old child.
{"title":"Giloy (Tinospora Cordifolia): A COVID-19 herbal drug causing erythroderma in a pediatric patient","authors":"Apoorva Gupta, M. Bansal, S. Gulati, Vatsala Gupta, Vinod K. Sharma","doi":"10.4103/ijpd.ijpd_75_22","DOIUrl":"https://doi.org/10.4103/ijpd.ijpd_75_22","url":null,"abstract":"Erythroderma or exfoliative dermatitis is characterized by erythema and scaling affecting more than 90% of the body surface area. Drug-induced erythrodermas are relatively uncommon in children but can be potentially life-threatening. We hereby report an unusual case of erythroderma due to oral intake of Giloy (Tinospora cordifolia) in a 10-year-old child.","PeriodicalId":13275,"journal":{"name":"Indian Journal of Paediatric Dermatology","volume":"24 1","pages":"167 - 170"},"PeriodicalIF":0.2,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42272747","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":"A rare case of bilateral xanthelasma palpebrarum in a 12-year-old girl","authors":"Aradhana Rout, A. K. Pandey","doi":"10.4103/ijpd.ijpd_46_22","DOIUrl":"https://doi.org/10.4103/ijpd.ijpd_46_22","url":null,"abstract":"","PeriodicalId":13275,"journal":{"name":"Indian Journal of Paediatric Dermatology","volume":"24 1","pages":"189 - 190"},"PeriodicalIF":0.2,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41683500","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}
Konchok Dorjay, M. Chauhan, Stanzin Dolker, Surabhi Sinha
{"title":"A case of multiple median raphe cysts with pathologically mixed variants: A rare presentation","authors":"Konchok Dorjay, M. Chauhan, Stanzin Dolker, Surabhi Sinha","doi":"10.4103/ijpd.ijpd_21_22","DOIUrl":"https://doi.org/10.4103/ijpd.ijpd_21_22","url":null,"abstract":"","PeriodicalId":13275,"journal":{"name":"Indian Journal of Paediatric Dermatology","volume":"24 1","pages":"204 - 205"},"PeriodicalIF":0.2,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48029506","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}
Vivek D Kumar, A. Bhatnagar, Karthi Kishore, D. Mitra
{"title":"SARS-CoV-2 infection-triggered juvenile dermatomyositis in a preschool male child: A rare presentation","authors":"Vivek D Kumar, A. Bhatnagar, Karthi Kishore, D. Mitra","doi":"10.4103/ijpd.ijpd_45_22","DOIUrl":"https://doi.org/10.4103/ijpd.ijpd_45_22","url":null,"abstract":"","PeriodicalId":13275,"journal":{"name":"Indian Journal of Paediatric Dermatology","volume":"24 1","pages":"191 - 192"},"PeriodicalIF":0.2,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47307518","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":"Midface toddler excoriation syndrome – A tale of scarring excoriation of the face","authors":"P. Gahalaut, Pravesh Valecha, Amarendra Singh","doi":"10.4103/ijpd.ijpd_37_22","DOIUrl":"https://doi.org/10.4103/ijpd.ijpd_37_22","url":null,"abstract":"","PeriodicalId":13275,"journal":{"name":"Indian Journal of Paediatric Dermatology","volume":"24 1","pages":"202 - 203"},"PeriodicalIF":0.2,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48758796","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}
Pub Date : 2023-04-01DOI: 10.4103/ijpd.ijpd_101_22
Phaneendra Kumar Manipudi, J. Logeshwari, Padmaja Pinjala, R. Thakur
{"title":"A case report of hereditary sensory and autonomic neuropathy – Type IV","authors":"Phaneendra Kumar Manipudi, J. Logeshwari, Padmaja Pinjala, R. Thakur","doi":"10.4103/ijpd.ijpd_101_22","DOIUrl":"https://doi.org/10.4103/ijpd.ijpd_101_22","url":null,"abstract":"","PeriodicalId":13275,"journal":{"name":"Indian Journal of Paediatric Dermatology","volume":"24 1","pages":"206 - 207"},"PeriodicalIF":0.2,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46203147","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}
Madam, Congenital anonychia is a rare disorder which might be either a part of a syndrome or an isolated occurrence.[1] Non-syndromic anonychia can be partial or total. Amniotic band syndrome (ABS) may present with a variety of congenital anomalies or as a very subtle, localized form.[2] ABS is due to rupture of the amnion early in pregnancy resulting in multiple loose strands called amniotic bands, that adhere to and may entangle the fetus as well.[3] Invasive procedures like chorionic villus sampling may lead this condition. We report a 3-day-old male neonate who presented with absence of all 10 toenails with normal fingernails, since birth. Constriction bands were present circumferentially in all toes, proximal to the areas of absent nails, and also over the ball of great toe on the left foot [Figures 1-3]. The fingernails were normal and there were no band-like depressions over them [Figure 4]. The baby was born by normal vaginal delivery as the first child of non-consanguineous parents and there was no history of any maternal drug intake, hypertension, or diabetes mellitus during pregnancy. The baby was otherwise normal with no other skin lesions or congenital anomalies. Radiology of feet showed no abnormality. Based on the clinical findings, a diagnosis of congenital anonychia due to amniotic constriction bands was made.Figure 1: Whitish areas representative of absent nails with ring-like constrictions proximallyFigure 2: Constriction rings on the plantar surfaceFigure 3: Bilaterally symmetrical involvement of both feetFigure 4: Normal fingernailsWhile the formation of amniotic bands in early gestation may lead to spontaneous abortions, in more advanced adanced gestation, classical rings, fissures, acro-syndactylization, or amputation of limbs may occur.[4] Clinically, constrictive rings, limb defects, neural or spine defects, and craniofacial defects are the four categories of presentation. Recently developed advanced three-dimensional ultrasound can diagnose these defects easily. Craniofacial abnormalities, such as encephalocele, cleft lip and palate, and spinal defects are rarely reported anomalies due to ABS. Most ABS cases are sporadic with no known recurrence risk unless in cases of familial ABS.[3] Our patient fortunately was mildly affected with only the absence of nails distal to the ring-like constrictions. This type of congenital nonsyndromic anonychia due to amniotic bands is a rare occurrence. Declaration of patient consent The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed. Financial support and sponsorship Nil. Conflicts of interest There are no conflicts of interest.
{"title":"Congenital Nonsyndromic Anonychia of Toes Due to Amniotic Bands","authors":"Abanti Bagchi, Asok Kumar Gangopadhyay, Nikhileswar Khawash, Sujata Sengupta, Swikruti Mohapatra","doi":"10.4103/ijpd.ijpd_91_22","DOIUrl":"https://doi.org/10.4103/ijpd.ijpd_91_22","url":null,"abstract":"Madam, Congenital anonychia is a rare disorder which might be either a part of a syndrome or an isolated occurrence.[1] Non-syndromic anonychia can be partial or total. Amniotic band syndrome (ABS) may present with a variety of congenital anomalies or as a very subtle, localized form.[2] ABS is due to rupture of the amnion early in pregnancy resulting in multiple loose strands called amniotic bands, that adhere to and may entangle the fetus as well.[3] Invasive procedures like chorionic villus sampling may lead this condition. We report a 3-day-old male neonate who presented with absence of all 10 toenails with normal fingernails, since birth. Constriction bands were present circumferentially in all toes, proximal to the areas of absent nails, and also over the ball of great toe on the left foot [Figures 1-3]. The fingernails were normal and there were no band-like depressions over them [Figure 4]. The baby was born by normal vaginal delivery as the first child of non-consanguineous parents and there was no history of any maternal drug intake, hypertension, or diabetes mellitus during pregnancy. The baby was otherwise normal with no other skin lesions or congenital anomalies. Radiology of feet showed no abnormality. Based on the clinical findings, a diagnosis of congenital anonychia due to amniotic constriction bands was made.Figure 1: Whitish areas representative of absent nails with ring-like constrictions proximallyFigure 2: Constriction rings on the plantar surfaceFigure 3: Bilaterally symmetrical involvement of both feetFigure 4: Normal fingernailsWhile the formation of amniotic bands in early gestation may lead to spontaneous abortions, in more advanced adanced gestation, classical rings, fissures, acro-syndactylization, or amputation of limbs may occur.[4] Clinically, constrictive rings, limb defects, neural or spine defects, and craniofacial defects are the four categories of presentation. Recently developed advanced three-dimensional ultrasound can diagnose these defects easily. Craniofacial abnormalities, such as encephalocele, cleft lip and palate, and spinal defects are rarely reported anomalies due to ABS. Most ABS cases are sporadic with no known recurrence risk unless in cases of familial ABS.[3] Our patient fortunately was mildly affected with only the absence of nails distal to the ring-like constrictions. This type of congenital nonsyndromic anonychia due to amniotic bands is a rare occurrence. Declaration of patient consent The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed. Financial support and sponsorship Nil. Conflicts of interest There are no conflicts of interest.","PeriodicalId":13275,"journal":{"name":"Indian Journal of Paediatric Dermatology","volume":"36 5 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136257709","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}
京公网安备 11010802042870号
京ICP备2023020795号-1
扫码关注我们
求助内容：
应助结果提醒方式：