Epidermolysis bullosa of the Dowling-Meara type: clinical and ultrastructural findings in five patients.

abstract：:Highly active antiretroviral therapy can restore specific immune responses and control of microorganism infections in human immunodeficiency virus-positive patients. This immune recovery may cause an inflammatory reaction to microbial and autoimmune antigens known as immune reconstitution inflammatory syndrome. We des...

journal_title：Pediatric dermatology

authors： de Carvalho VO,Cruz CR,Noronha L,Abagge KT,Lima HC

更新日期：2010-11-01 00:00:00

abstract：:We cared for 124 pediatric patients with a histologic diagnosis of Langerhans' cell histiocytosis (histiocytosis X) over a period of 14 years. Clinical, laboratory, and radiographic findings were analyzed. The most frequent manifestations were bone lesions, lymph node involvement, and skin infiltration. Liver disease ...

journal_title：Pediatric dermatology

authors： Rivera-Luna R,Martinez-Guerra G,Altamirano-Alvarez E,Martinez-Avalos A,Cardenas-Cardoz R,Ayon-Cardenas A,Ruiz-Maldonado R,Lopez-Corella E

更新日期：1988-08-01 00:00:00

abstract：:Hidradenitis suppurativa is a chronic relapsing disorder of follicular occlusion that is often recalcitrant to therapy. Topical and systemic antibiotics, hormonal therapies, oral retinoids, immunosuppressant agents, and surgical treatment are some of the therapeutic alternatives used for this often recalcitrant and fr...

journal_title：Pediatric dermatology

authors： Lam J,Krakowski AC,Friedlander SF

更新日期：2007-09-01 00:00:00

abstract：:Epidermolysis bullosa acquisita (EBA) is a rare, acquired, subepidermal blistering disease characterized by autoantibodies directed against type VII collagen, the major component of anchoring fibrils. We report a 5-year-old Chinese boy who presented with extensive lesions consisting of disseminated pruritic vesicles a...

journal_title：Pediatric dermatology

authors： Yang B,Wang C,Wang N,Pan F,Chen S,Zhou G,Yu M,Zhang F

更新日期：2012-09-01 00:00:00

abstract：:A new type of organoid epidermal nevus, characterized by the presence of multiple trichilemmal cysts disposed in a linear arrangement, was recently recognized and named nevus trichilemmocysticus. We report a 10-year-old girl with a congenital linear dermatosis affecting the head, neck, trunk, limbs, palms, and soles. ...

journal_title：Pediatric dermatology

authors： Larralde M,Boggio P,Abad ME,Corbella C,Happle R

更新日期：2011-05-01 00:00:00

abstract：:Midline congenital cervical cleft is an extremely uncommon anomaly of the neck. Fewer than 100 cases have been reported. It is usually described as a cervical scar-like skin defect. We present a case of midline cervical cleft mimicking linear morphea and treated with topical steroids for 2 years. This is an unusual pr...

journal_title：Pediatric dermatology

authors： Méndez-Gallart R,Martinez EE,Rodríguez-Barca P,Nallib IA,Bautista-Casasnovas A

更新日期：2013-07-01 00:00:00

abstract：:Loose anagen hair syndrome (LAHS) is an uncommonly reported autosomal dominant hair disorder with incomplete penetrance that primarily affects children but is occasionally seen in adults. LAHS is characterized by the ability to easily and painlessly extract unsheathed anagen hairs from the scalp with gentle traction. ...

journal_title：Pediatric dermatology

authors： Dey V,Thawani M

更新日期：2013-09-01 00:00:00

abstract：:Nipple adenoma is an uncommon proliferative process of the breast and predominantly occurs in women aged 40-50. Its incidence is extremely low in men, and it has not been reported in a boy. Although nipple adenoma is rare and benign, being familiar with it is important because it clinically resembles Paget disease and...

journal_title：Pediatric dermatology

authors： Fujisawa K,Kato M,Kono T,Utsunomiya H,Watanabe A,Watanabe S

更新日期：2018-05-01 00:00:00

abstract：:Poikiloderma with neutropenia (PN), Clericuzio type (OMIM #604173) is a new, unique genodermatosis first described by Clericuzio et al (Am J Med Genet A, 2011, 155, 337) in Navajo Indian population. This disease is characterized by poikiloderma that usually develops in the first year of life and is associated with nai...

journal_title：Pediatric dermatology

authors： Chantorn R,Shwayder T

更新日期：2012-07-01 00:00:00

abstract：:We report a case of a young man with perforating folliculitis and cystic fibrosis with complications including chronic obstructive pulmonary disease, insulin dependent diabetes mellitus, and liver cirrhosis. We demonstrate increased TGF-β1 immunohistochemical staining in the perforating folliculitis lesions of our pat...

journal_title：Pediatric dermatology

authors： Tuttle MS,Kwon EJ,Tamburro J,Honda K

更新日期：2010-11-01 00:00:00

abstract：:Prurigo pigmentosa (PP) is a rare inflammatory skin disease. Neutrophil-mediated inflammation is considered to be responsible for the etiopathogenesis of PP. We consider that colchicine may be an effective agent in the treatment of PP since it exerts an antiinflammatory effect by inhibiting neutrophil chemotaxis. Furt...

journal_title：Pediatric dermatology

authors： An I,Ucmak D,Ibiloglu I,Demir V,Akdeniz S

更新日期：2018-05-01 00:00:00

abstract：:Autosomal recessive congenital ichthyosis is a genetically and phenotypically heterogenous group of scaling skin disorders. We describe a patient with ARCI caused by homozygous variants in NIPAL4, in whom the dermatologic phenotype and an associated arthropathy, markedly improved with ustekinumab. ...

journal_title：Pediatric dermatology

authors： Poulton C,Gration D,Murray K,Baynam G,Halbert A

更新日期：2019-11-01 00:00:00

abstract：:We report a child with bilateral congenital triangular alopecia. Shaving the scalp and inserting intravenous cannulas into scalp vessels during the neonatal period was misconstrued by the parents as the cause of hair loss, and resulted in medicolegal implications. ...

journal_title：Pediatric dermatology

authors： Armstrong DK,Burrows D

更新日期：1996-09-01 00:00:00

abstract：:Clinical aspects of sequestrated meningocele can be varied, causing difficulties in histopathological diagnosis. The meningeal tissue is scanty and appears as nonspecific connective tissue, therefore it may be overlooked. One classical and two unusual clinical presentations of sequestrated meningocele are described: o...

journal_title：Pediatric dermatology

authors： Khallouf R,Fétissof F,Machet MC,Stephanov E,Lechrist J,Lorette G

更新日期：1994-12-01 00:00:00

abstract：:Infantile myofibromatosis is a rare benign tumor of infancy and childhood that occurs in solitary, multiple, and generalized forms with similar histology but different clinicopathologic and prognostic implications. Even solitary tumors need follow-up, as the type of presentation will be determined over time. It is nec...

journal_title：Pediatric dermatology

authors： Jurcić V,Perković T,Pohar-Marinsek Z,Hvala A,Lazar I

更新日期：2003-07-01 00:00:00

abstract：:Aplasia cutis congenita (ACC) is a congenital defect consisting of a circumscribed absence of skin that usually involves the scalp. The etiology is uncertain, and several teratogenic agents such as methimazole have been involved. We report two cases of ACC and other anomalies in newborns exposed to methimazole during ...

journal_title：Pediatric dermatology

authors： Rodríguez-García C,González-Hernández S,Hernández-Martín A,Pérez-Robayna N,Sánchez R,Torrelo A

更新日期：2011-11-01 00:00:00

abstract：:Although the U.S. pediatric skin care market is a $1.7 billion industry, little is known regarding the usage pattern of skin care products in very young children. We have begun to recognize that common over-the-counter skin care products may have positive or negative effects on skin barrier function. Thus, knowing wha...

journal_title：Pediatric dermatology

authors： Gao X,Simpson EL

更新日期：2014-11-01 00:00:00

abstract：:The disorders of cornification (ichthyoses) comprise acquired and inherited disorders characterized clinically by generalized scaling and histologically by hyperkeratosis. They may arise through defects in the production or maintenance of a normal cornified cell compartment, or both. The stratum corneum is composed of...

journal_title：Pediatric dermatology

authors： Williams ML

更新日期：1992-12-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Palmar hyperlinearity is a typical clinical feature of Filaggrin gene (FLG) null mutations. There are reports of FLG mutations and allergic sensitization; however, reports on the relationship between palmar hyperlinearity to sensitization are limited. This study aimed to examine the association be...

journal_title：Pediatric dermatology

authors： Fukuie T,Yasuoka R,Fujiyama T,Sakabe JI,Taguchi T,Tokura Y

更新日期：2019-03-01 00:00:00

abstract：:Graft-versus-host disease (GVHD) is an underappreciated complication of autologous hematopoietic stem cell transplantation (AHSCT) that can affect the skin, gastrointestinal tract, and liver. The development of this rare condition is probably due to an impairment of immunologic tolerance that can occur spontaneously t...

journal_title：Pediatric dermatology

authors： Kaffenberger J,Basak SA,Ioffreda M

更新日期：2015-03-01 00:00:00

abstract：:Aplasia cutis congenita (ACC) is characterized by the complete or partial absence of skin at birth, with 85% of cases of ACC involving the scalp vertex. The etiology of ACC is unclear and appears to be multifactorial. We present the case of a 3-month-old boy who presented with a diagnosis of non-scalp ACC affecting ap...

journal_title：Pediatric dermatology

authors： Davis MJ,Voller LM,Gonzalez SR,Abu-Ghname A,Davies LW,Bedwell JR,Lee GL,Hunt RD,Phung TL,Buchanan EP

更新日期：2021-01-22 00:00:00

abstract：:We report an Italian prepubescent girl with the typical clinical and histologic features of prurigo pigmentosa associated with an atopic diathesis. The dermatitis disappeared after treatment with minocycline, leaving a brown, reticulated hyperpigmentation, with no recurrence. The association with an atopic diathesis c...

journal_title：Pediatric dermatology

authors： Cota C,Donati P,Amantea A

更新日期：2007-05-01 00:00:00

abstract：:Although papulonecrotic tuberculid is an uncommon cutaneous manifestation of tuberculosis (TB) associated with Mycobacterium tuberculosis infection, the simultaneous occurrence of papulonecrotic tuberculid and erythema induratum is even rarer. Papulonecrotic tuberculid occurs predominantly in young adults and is chara...

journal_title：Pediatric dermatology

authors： Kim GW,Park HJ,Kim HS,Chin HW,Kim SH,Ko HC,Kim MB,Kim BS

更新日期：2013-03-01 00:00:00

abstract：:Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive disorder that is caused by a DNA repair defect. It is characterized mainly by skin, eye, and skeletal abnormalities. Cutaneous changes appear at between 3 and 6 months of age and include poikiloderma, photosensitivity, scaling, hyperkeratosis, and disturban...

journal_title：Pediatric dermatology

authors： Narayan S,Fleming C,Trainer AH,Craig JA

更新日期：2001-05-01 00:00:00

abstract：:A 14-year-old boy presented with extensive capillaritis. Narrow-band ultraviolet B was administered on a thrice-weekly schedule followed by once-a-week maintenance. A favorable response to treatment was seen without any side effects. ...

journal_title：Pediatric dermatology

authors： Verma P

更新日期：2013-11-01 00:00:00

abstract：BACKGROUND:Phosphodiesterase-4 (PDE4) is a promising target in atopic dermatitis (AD) treatment. The pharmacokinetics (PK), safety, and efficacy of crisaborole topical ointment, 2% (formerly AN2728) (Anacor Pharmaceuticals, Palo Alto, CA), a boron-based benzoxaborole PDE4 inhibitor, were evaluated in children with mild...

journal_title：Pediatric dermatology

authors： Zane LT,Kircik L,Call R,Tschen E,Draelos ZD,Chanda S,Van Syoc M,Hebert AA

更新日期：2016-07-01 00:00:00

abstract：:Parry-Romberg syndrome (PRS) is characterized by hemiatrophy of facial structures, including skin, subcutaneous fat, muscle, bone, and cartilage. Complications associated with PRS include headaches, seizures, and chronic facial pain. Protocol for the treatment of chronic facial pain is not clear; reports on the use of...

journal_title：Pediatric dermatology

authors： Mishra K,Sood A,Smidt A,Price HN

更新日期：2019-03-01 00:00:00

abstract：:We describe the clinicopathologic features of an unusual case of fibromatosis colli. The lesion was rock hard, lateral, tightly affixed to the clavicle, and with overlying hypertrichosis. ...

journal_title：Pediatric dermatology

authors： Amin A,Loftis B,Shwayder TA

更新日期：2010-09-01 00:00:00

abstract：:A new consensus-based classification of congenital melanocytic nevi (CMN) has recently been proposed. It includes categories for projected adult size (PAS) and location, satellite nevi counts, and morphologic characteristics (color heterogeneity, rugosity, nodularity, and hypertrichosis). The objective of the current ...

journal_title：Pediatric dermatology

authors： Price HN,O'Haver J,Marghoob A,Badger K,Etchevers H,Krengel S

更新日期：2015-01-01 00:00:00

abstract：:We report a case of congenital hypertrichosis and FOXN1 duplication. FOXN1 is a member of the forkhead box gene family, located on chromosome 17. Its function includes differentiation of epithelial cells and regulation of keratinocytes, especially hair keratins. Loss of function of these transcription factors leads to...

journal_title：Pediatric dermatology

authors： Gilhooley E,Gormally S,Irvine A,Lynch SA,Collins S

更新日期：2017-03-01 00:00:00