Serum sickness-like reaction in children due to cefditoren.


:We describe the case of a 7-year-old boy with urticaria, fever, and arthritis that appeared 10 days after starting cefditoren therapy for acute tonsillopharyngitis, which was diagnosed as a serum sickness-like reaction due to this medication.


Pediatr Dermatol


Pediatric dermatology


Misirlioglu ED,Duman H,Ozmen S,Bostanci I




Has Abstract


2012-05-01 00:00:00












  • Transient Porphyrinemia in a Neonate: A Case Report.

    abstract::We describe a neonate with anemia, thrombocytopenia, and hyperbilirubinemia secondary to hemolytic disease of the newborn. After phototherapy for hyperbilirubinemia, the neonate developed a photodistributed eruption with high serum and urine porphyrin levels. This transient porphyrinemia resolved at 1 month. ...

    journal_title:Pediatric dermatology



    authors: Boer B,Tisack A,Shwayder T

    更新日期:2016-11-01 00:00:00

  • Depilation in a 6-month-Old with hypertrichosis: A case report.

    abstract::Hypertrichosis in the pediatric age group can be troubling to both patients and parents. There is no well-established method for managing this problem in young children. We describe the successful use of a cream depilatory agent for removal of excess hair from the face and body of a 6-month-old girl. Excellent cosmeti...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Wendelin DS,Mallory GB,Mallory SB

    更新日期:1999-07-01 00:00:00

  • Childhood onset vulvar lichen sclerosus does not resolve at puberty: a prospective case series.

    abstract::When vulvar lichen sclerosus occurs in prepubertal children it is widely believed that it is likely to remit at puberty. However when it occurs in adult women it is accepted that remission is unlikely and that in addition untreated or inadequately treated disease may be complicated by significant disturbance of vulvar...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Smith SD,Fischer G

    更新日期:2009-11-01 00:00:00

  • Loose anagen hair syndrome in black-haired Indian children.

    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

    pub_type: 杂志文章


    authors: Dey V,Thawani M

    更新日期:2013-09-01 00:00:00

  • Acute ulceronecrotic adverse reaction to potassium hydroxide 5% solution in the treatment of molluscum contagiosum.

    abstract::Molluscum contagiosum is a common childhood condition, and although it is self-limited, treatments are often prescribed. Several medications are available, but there is no consensus regarding the optimal choice in the pediatric population. We report a child who underwent potassium hydroxide 5% treatment resulting in s...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Bresesti I,Ciolfi C,Rotatore G,Borisov AN,Zuccotti GV,Brazzelli V

    更新日期:2020-01-01 00:00:00

  • Frequency and severity of diaper dermatitis with use of traditional Chinese cloth diapers: observations in 3- to 9-month-old children.

    abstract::Chinese cloth diapers differ from disposable diapers in several respects that are central to our understanding of the etiology of diaper dermatitis (DD), yet there are no published reports on the dermatological correlates of this manner of infant care, which is prevalent among the world's second-largest pediatric popu...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Liu N,Wang X,Odio M

    更新日期:2011-07-01 00:00:00

  • Radiation Recall Dermatitis Secondary to Dactinomycin.

    abstract::Radiation recall dermatitis (RRD) is an uncommon reaction typically triggered by the use of chemotherapeutic agents in the months after treatment with radiation therapy. It usually presents as dermatitis in the irradiated field with prominent intertriginous involvement, and because internal involvement occurs in up to...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Prindaville B,Horii KA,Canty KM

    更新日期:2016-09-01 00:00:00

  • Perianal streptococcal dermatitis associated with guttate psoriasis and/or balanoposthitis: a study of five cases.

    abstract::Perianal streptococcal dermatitis (PSD) is a recently described cutaneous entity caused by group A beta-hemolytic streptococci. It is characterized by perianal erythema, sometimes associated with functional disturbances. We describe four children (2 boys, 2 girls) who had acute guttate psoriasis and also PSD. One of t...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Patrizi A,Costa AM,Fiorillo L,Neri I

    更新日期:1994-06-01 00:00:00

  • Hidradenitis suppurativa (acne inversa): management of a recalcitrant disease.

    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

    pub_type: 杂志文章,评审


    authors: Lam J,Krakowski AC,Friedlander SF

    更新日期:2007-09-01 00:00:00

  • Melanocytic nevi in Turner syndrome.

    abstract::One morphologic feature of Turner syndrome is increased numbers of melanocytic nevi; however, little attention has been given to their characterization. The development of a melanoma in one of our patients with Turner syndrome prompted this study. We prospectively examined 10 patients with the disease, confirmed by ka...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Becker B,Jospe N,Goldsmith LA

    更新日期:1994-06-01 00:00:00

  • Subcutaneous fat necrosis in two infants after hypothermic cardiac surgery.

    abstract::Two infants experienced subcutaneous fat necrosis (SCFN) at a relatively late age after cardiac surgery with induced hypothermia. The condition resolved in both patients over four weeks without treatment. The appearance of SCFN after the newborn period is very unusual, and in these patients was probably related to the...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Glover MT,Catterall MD,Atherton DJ

    更新日期:1991-09-01 00:00:00

  • Childhood lichen planus: a report of 23 cases.

    abstract::Lichen planus (LP) in children is a rare entity. We report 23 cases of childhood LP seen over a period of 7 years. Ninety-six percent of the children were of Arab ancestry. There were 52% boys and 48% girls. Classic LP was the most common clinical variant (70%), followed by eruptive generalized LP (13%). A majority of...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Nanda A,Al-Ajmi HS,Al-Sabah H,Al-Hasawi F,Alsaleh QA

    更新日期:2001-01-01 00:00:00

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

    abstract::Clinical and pathologic features of five cases of epidermolysis bullosa simplex, Dowling-Meara type (EBS-DM), are described. Four patients were children, and two were related (father and daughter). Clinical history revealed blistering at birth in three patients; in all of them the signs and symptoms improved with age....

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Puddu P,Angelo C,Faraggiana T,Onetti Muda A,Colonna L,Paradisi M

    更新日期:1996-05-01 00:00:00

  • Simultaneous occurrence of papulonecrotic tuberculid and erythema induratum in a patient with pulmonary tuberculosis.

    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

    pub_type: 杂志文章


    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

  • A survey to assess use patterns and perceptions of efficacy of eczema action plans among pediatric dermatologists.

    abstract::Eczema action plans (EAPs) are written, customizable documents that guide patients through the self-management of atopic dermatitis. Here, we distributed a survey regarding the use patterns and perceptions of eczema action plans to 1068 members of the Society for Pediatric Dermatology and received 87 responses. Althou...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Stringer T,Yin HS,Oza VS

    更新日期:2018-11-01 00:00:00

  • Ruvalcaba-Myhre-Smith syndrome.

    abstract::In 1980 a syndrome was first described in two adult males, consisting of macrocephaly, pigmented macules on the glans and shaft of the penis, and hamartomatous intestinal polyps. Since then, 10 additional cases have been identified. Herein, we present two new cases and review the cutaneous manifestations as well as ad...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Gretzula JC,Hevia O,Schachner LS,DiLiberti JH,Ruvalcaba RH,Schimschock JR,Weleber RG,Halal F,Lipson MH,Blumberg B

    更新日期:1988-02-01 00:00:00

  • Prevalence of inflammatory bowel disease among pediatric patients with hidradenitis suppurativa and the potential role of screening with fecal calprotectin.

    abstract:BACKGROUND/OBJECTIVES:Previous studies have demonstrated an increased prevalence of inflammatory bowel disease (IBD) in adults with hidradenitis suppurativa (HS). Whether the same association exists in pediatric patients is unknown. Fecal calprotectin (FC) is used to screen and monitor disease activity in IBD. There ar...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Lloyd-McLennan AM,Ali S,Kittler NW

    更新日期:2020-10-25 00:00:00

  • An unusual case of infantile dermal mucinosis.

    abstract::Dermal mucinosis occurred in a 3-month-old and persisted for six years. The features suggest is represents a novel type of childhood mucinosis. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Calza AM,Masouyé I,Saurat JH

    更新日期:1994-09-01 00:00:00

  • Halolike Phenomenon Around a Café au Lait Spot Superimposed on a Mongolian Spot.

    abstract::An 8-month-old Caucasian infant with neurofibromatosis type 1 presented with a congenital plexiform neurofibroma and multiple café au lait spots. A pale area surrounded one of the café au lait spots located on the left gluteus in the area of dermal melanocytosis. This halolike phenomenon results from the disappearance...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Neri I,Lambertini M,Tengattini V,Rivalta B,Patrizi A

    更新日期:2017-05-01 00:00:00

  • Erythema nodosum in association with celiac disease.

    abstract::We present a 16-year-old girl with a 4-year history of chronic persistent erythema nodosum. Recurrently low serum iron values suggested the possibility of a malabsorption syndrome. The presence of antitransglutaminase and antiendomysium antibodies and the jejunal biopsy specimen findings showed an underlying celiac di...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Bartyik K,Várkonyi A,Kirschner A,Endreffy E,Túri S,Karg E

    更新日期:2004-05-01 00:00:00

  • Profile and outcome of childhood mycosis fungoides in Singapore.

    abstract::Mycosis fungoides (MF) is the most common form of cutaneous T-cell lymphoma. It usually occurs in middle-aged and elderly persons, although several reports have described its occurrence in young children. The aim of this study was to review the profile and outcome of childhood MF in Singapore from 1989 to 1998. A tota...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Tan E,Tay YK,Giam YC

    更新日期:2000-09-01 00:00:00

  • Fatal nodular xanthomatosis in an infant.

    abstract::We describe a unique and puzzling case of a 7-month-old baby with a non-X hypertriglyceridemic histiocytoxanthomatosis. The disease was characterized by a massive nodular eruption that was clinically, histologically, and ultrastructurally consistent with juvenile xanthogranuloma, but it had a rapid, fatal evolution. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Caputo R,Ermacora E,Gelmetti C,Gianni E

    更新日期:1987-11-01 00:00:00

  • Perforating folliculitis in a patient with cystic fibrosis.

    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

    pub_type: 杂志文章


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

    更新日期:2010-11-01 00:00:00

  • Perianal striated muscle hamartoma associated with hemangioma.

    abstract::Striated muscle hamartoma is a rare entity which was described only recently. It is a congenital malformation characterized by the presence of striated, mature muscle fibers in the reticular dermis and hypodermis. We describe a striated muscle hamartoma of the perianal region in a female infant associated with an hema...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审


    authors: Scrivener Y,Petiau P,Rodier-Bruant C,Cribier B,Heid E,Grosshans E

    更新日期:1998-07-01 00:00:00

  • Evolution of congenital melanocytic nevi toward benignity: A case series.

    abstract::We report on four children born with medium to large congenital melanocytic nevi (CMN) with color heterogeneity and irregular surface rugosity. As these patients aged, their nevi evolved to become more homogeneous and lighter in color, and developed a smoother, more even texture. We propose that given this evolution t...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Cotton CH,Goldberg GN

    更新日期:2019-03-01 00:00:00

  • Congenital curved nail of the fourth toe--three different clinical presentations.

    abstract::A congenital curved nail of the fourth toe (NIM 219070) is a rare nail deformity with no other associated abnormalities. Three patients with this congenital anomaly are reported here. Radiologic examination in all three revealed distal symphalangism of the fourth toes bilaterally. The clinical manifestations in these ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Lin YC,Wu YH,Scher RK

    更新日期:2007-07-01 00:00:00

  • Anti-Ku antibody-positive systemic sclerosis-polymyositis overlap syndrome in an adolescent.

    abstract::Systemic sclerosis-polymyositis overlap syndrome is rare in children. Anti-PM/Scl is the most common autoantibody associated with this syndrome. We present a case of systemic sclerosis-polymyositis overlap syndrome in a child with isolated anti-Ku antibodies, an uncommon antibody associated with this rare syndrome. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Loo RJ,Nocton JJ,Harmelink MM,Chiu YE

    更新日期:2020-09-01 00:00:00

  • Sun exposure and protection practices in children after allogeneic hematopoietic stem cell transplantation: A Survey-Based Cross-Sectional Cohort Study.

    abstract:BACKGROUND/OBJECTIVE:Pediatric hematopoietic stem cell transplantation (HSCT) patients are at an increased risk for skin cancers. Sun exposure is a significant modifiable environmental risk factor. While patient education on sun protection and avoidance behaviors with regular dermatology evaluations are crucial for ped...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Li EB,Song JS,Huang JT,Hawryluk EB,London WB,Guo D,Sridharan M,Fisher DE,Rea CJ,Lehmann LE,Duncan CN

    更新日期:2019-11-01 00:00:00

  • Cutaneous histiocytosis syndromes.

    abstract::Cutaneous histiocytosis may take two principal forms. It is either a benign proliferative process or a relentless, progressive process with a poor prognosis. In histiocytic medullary reticulosis, histiocytes demonstrate nuclear atypia and the outcome is uniformly fatal. Benign cephalic histiocytosis X causes lesions s...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审


    authors: Roper SS,Spraker MK

    更新日期:1985-11-01 00:00:00

  • Diffuse capillary malformation in association with fetal pleural effusion: report of five patients.

    abstract::Capillary malformation (CM) can be a "red flag" for several syndromic vascular anomalies. We identified a subset of patients with diffuse CM and fetal pleural effusion and documented the type of CM, the etiology of the pleural effusion, the potential syndromic diagnosis, and outcome. Patients with a history of CM and ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章


    authors: Rork JF,Alomari AI,Mulliken JB,Fishman SJ,Liang MG

    更新日期:2015-01-01 00:00:00