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  • 1
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2014
    In:  Dermatology and Therapy Vol. 4, No. 1 ( 2014-6), p. 131-135
    In: Dermatology and Therapy, Springer Science and Business Media LLC, Vol. 4, No. 1 ( 2014-6), p. 131-135
    Type of Medium: Online Resource
    ISSN: 2193-8210 , 2190-9172
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2014
    detail.hit.zdb_id: 2680284-3
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  • 2
    Online Resource
    Online Resource
    SAGE Publications ; 2010
    In:  Rare Tumors Vol. 2, No. 2 ( 2010-06-30), p. 94-96
    In: Rare Tumors, SAGE Publications, Vol. 2, No. 2 ( 2010-06-30), p. 94-96
    Abstract: Langerhans cell histiocytosis is a rare group of proliferative disorders. Beside cutaneous involvement, other internal organs can be affected. The treatment of cutaneous lesions is difficult and relies on topical corticosteroids, carmustine, nitrogen mustard, and photochemotherapy. Systemic steroids and vinblastine are used for recalcitrant skin lesions. However, some cases fail to respond. An 18-month old boy presented a CD1a + , S100a + Langerhans cell histocytosis with cutaneous and severe scalp involvement. Topical corticosteroids and nitrogen mustard failed to improve the skin lesions. Systemic corticosteroids and vinblastine improved the truncal involvement but had no effect on the scalp lesions. Methylaminolevulinate (MAL) based photodynamic therapy (PDT) resulted in a significant regression of the scalp lesions. Control histology revealed an almost complete clearance of the tumor infiltrate. Clinical follow-up after six months showed no recurrence. Although spontaneous regression of cutaneous Langerhans cell histiocytosis is observed, the rapid effect of photodynamic therapy after several failures of other treatment suggests that photodynamic therapy was successful. As far as we know this is the first report of photodynamic therapy for refractory skin lesions. Larger series are needed to determine whether photodynamic therapy deserves a place in the treatment of multiresistant cutaneous Langerhans cell histiocytosis.
    Type of Medium: Online Resource
    ISSN: 2036-3613 , 2036-3613
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2010
    detail.hit.zdb_id: 2514363-3
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  • 3
    Online Resource
    Online Resource
    Wiley ; 2004
    In:  Pediatric Dermatology Vol. 21, No. 1 ( 2004-01), p. 18-23
    In: Pediatric Dermatology, Wiley, Vol. 21, No. 1 ( 2004-01), p. 18-23
    Abstract: Abstract:  Herpes zoster is rare in otherwise healthy children, but it is more common in association with immunosuppression. Maternal varicella infection during pregnancy and varicella occurring in the newborn represent risk factors for childhood herpes zoster. However, some controversies persist about risk factors, diagnosis, and the natural history of childhood disease. In a 2‐year prospective study, 18 children with herpes zoster were clinically diagnosed in outpatient consultations in a hospital dermatology unit. Data about age, dermatome involvement, underlying disease, and history of previous varicella were recorded. Tzanck smears, biopsy specimens, and sera were obtained from 18, 4, and 10 children, respectively. The varicella zoster virus major envelope glycoprotein gE was detected in 16 of 18 smears and all four biopsies. Herpes simplex virus I was demonstrated in one of the smears. The established risk factors for childhood herpes zoster were only found in one child. Evidence for previous full‐blown varicella and varicella with few lesions was recorded in 7 and 4 of the 17 immunocompetent children, respectively. No history of varicella was recalled in 6 of 17 cases, although a serologic clue of past varicella infection (IgM negative, IgG positive) was disclosed. Recurrent herpes zoster was diagnosed in one immunocompromised child. Zoster‐associated pain was localized and the disease severity remained mild in all children. Established risk factors for childhood herpes zoster were only rarely found in our series of patients. In contrast, unrecognized varicella and varicella with few lesions were frequently recorded and may represent additional risk factors for shingles in childhood. Zosteriform herpes simplex virus infections should be differentiated from childhood herpes zoster, emphasizing the importance of precise viral identification.
    Type of Medium: Online Resource
    ISSN: 0736-8046 , 1525-1470
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2004
    detail.hit.zdb_id: 605539-4
    detail.hit.zdb_id: 2020833-9
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  • 4
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2016
    In:  Melanoma Research Vol. 26, No. 6 ( 2016-12), p. 631-634
    In: Melanoma Research, Ovid Technologies (Wolters Kluwer Health), Vol. 26, No. 6 ( 2016-12), p. 631-634
    Abstract: Increased awareness among dermatologists as well as the development of dermoscopy and sequential dermoscopy have contributed significantly toward an increase in the diagnostic accuracy of pigmented melanoma and even of amelanotic melanoma. However, the dermatologist’s nightmare is the small group of melanomas that present as common skin diseases, often associated with a significant delay in diagnosis and hence a poor prognosis. The study was carried out to prospectively assess the number of melanomas lacking any clinical suspicion of melanoma and to describe their clinical and histological features over a 6-year observation period in an University Tertiary Skin Cancer Center. Out of 502 cases of newly diagnosed cases of melanoma, seven (1.4%) nonpigmented and nonamelanotic cases of melanoma were identified. The mean age of the patients was 69 years (two females/five males). All cases were discovered by chance on a punch biopsy. The clinical diagnostic suspicions were basal cell carcinoma, fungal intertrigo, keratoacanthoma, lichenoid keratoma, diabetic foot ulcer, eczema, and necrotic pressure ulcer. Dermoscopy, performed after the punch biopsies, was only partially contributive. The mean histological thickness was 2.7 mm, the mean number of mitoses was 7/mm 2 , local micrometastases were present in 5/7 (71%), the mean Ki67 count was 18.9%, and a positive sentinel lymph node was observed in 4/6 (66%) cases. Nonpigmented and nonamelanotic melanomas are rare, are at high risk, and have a poor prognosis because of a delayed diagnosis. Dermoscopy is only of partial diagnostic aid. Treatment resistance or atypical behavior of the above-mentioned lesions should lead to biopsy.
    Type of Medium: Online Resource
    ISSN: 0960-8931
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2016
    detail.hit.zdb_id: 1095779-0
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  • 5
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2006
    In:  American Journal of Clinical Dermatology Vol. 7, No. 5 ( 2006), p. 327-331
    In: American Journal of Clinical Dermatology, Springer Science and Business Media LLC, Vol. 7, No. 5 ( 2006), p. 327-331
    Type of Medium: Online Resource
    ISSN: 1175-0561
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2006
    detail.hit.zdb_id: 1502476-3
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  • 6
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2005
    In:  American Journal of Clinical Dermatology Vol. 6, No. 2 ( 2005), p. 79-87
    In: American Journal of Clinical Dermatology, Springer Science and Business Media LLC, Vol. 6, No. 2 ( 2005), p. 79-87
    Type of Medium: Online Resource
    ISSN: 1175-0561
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2005
    detail.hit.zdb_id: 1502476-3
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  • 7
    In: Rare Tumors, SAGE Publications, Vol. 1, No. 2 ( 2009-12-28), p. 146-147
    Abstract: Infantile digital fibromatosis (IDF) is a rare benign fibroproliferative tumor of early childhood. IDF preferentially affects the fingers and the toes. Malignant transformation or metastases have never been reported. Surgical treatment has been advocated previously but local recurrences were observed frequently. Recent literature supports clinical surveillance without any medical or surgical intervention as spontaneous regression usually occurs after two to three years. A six-month-old Caucasian girl with IDF on the left fourth digit is presented here. The tumor progressively increased in size after birth. Topical imiquimod cream and diflucortolone valerate cream, both displaying antifibrotic properties, had no effect on tumor growth. Currently the lesion size remains stable without any treatment. Early recognition of IDF is important in order to avoid unnecessary surgical intervention that may prove to be potentially aggravating, unless serious functional or cosmetic concerns intervene. Parents should be reassured concerning the benign nature of IDF and be informed that spontaneous involution of IDF might be expected.
    Type of Medium: Online Resource
    ISSN: 2036-3613 , 2036-3613
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2009
    detail.hit.zdb_id: 2514363-3
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  • 8
    Online Resource
    Online Resource
    S. Karger AG ; 2013
    In:  Case Reports in Dermatology Vol. 5, No. 1 ( 2013-2-21), p. 43-47
    In: Case Reports in Dermatology, S. Karger AG, Vol. 5, No. 1 ( 2013-2-21), p. 43-47
    Abstract: Varicella zoster virus (VZV) cutaneous infection occurs predominantly in epidermal and infundibular keratinocytes and accessorily in dermal dendritic cells. These latter cells play a role in cicatricial processes. Two patients are presented with localized alopecia after VZV infection. A 4-year-old girl presented localized hair loss affecting about 20% of her upper right eyelash immediately following the resolution of the varicella skin lesions. No regrowth was observed after 3 months. An 80-year-old woman with a prior history of localized alopecia areata of the left occipital area presented severe left herpes zoster affecting the V1 and V2 dermatomes. At precisely the same site of the previous episode, a localized plaque of alopecia areata recurred. After topical corticosteroid therapy, a progressive hair regrowth occurred after about 3 months. These case reports are the first relating cutaneous VZV infection as the origin for permanent cicatricial alopecia and transitory alopecia areata. Localized hair loss should be added to the cutaneous complications of VZV skin infection.
    Type of Medium: Online Resource
    ISSN: 1662-6567
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2013
    detail.hit.zdb_id: 2505300-0
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  • 9
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2018
    In:  American Journal of Clinical Dermatology Vol. 19, No. 6 ( 2018-12), p. 893-897
    In: American Journal of Clinical Dermatology, Springer Science and Business Media LLC, Vol. 19, No. 6 ( 2018-12), p. 893-897
    Type of Medium: Online Resource
    ISSN: 1175-0561 , 1179-1888
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2018
    detail.hit.zdb_id: 1502476-3
    detail.hit.zdb_id: 2043675-0
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  • 10
    Online Resource
    Online Resource
    S. Karger AG ; 2013
    In:  Kompass Dermatologie Vol. 1, No. 1 ( 2013), p. 49-51
    In: Kompass Dermatologie, S. Karger AG, Vol. 1, No. 1 ( 2013), p. 49-51
    Abstract: Die kutane Varicella-Zoster-Virus(VZV)-Infektion tritt überwiegend in epidermalen und infundibulären Keratinozyten sowie in dermalen dendritischen Zellen auf. Letztere spielen bei Vernarbungsprozessen eine Rolle.Zwei Patienten mit lokalisierter Alopezie nach VZV-Infektion werden vorgestellt. Ein 4-jähriges Mädchen zeigte lokalisierten Haarausfall, der etwa 20% der Wimpern am rechten Oberlid betraf und unmittelbar nach Abheilung der Varicella-Hautläsionen auftrat. Nach 3 Monaten war kein Nachwachsen zu beobachten. Eine 80-jährige Frau mit lokalisierter Alopecia areata der linken Okzipitalregion in der Vorgeschichte stellte sich mit schwerem linksseitigen Herpes zoster im Bereich der Dermatome V1 und V2 vor. An der exakt gleichen Stelle wie bei der vorherigen Episode trat erneut ein lokalisierter Alopecia-areata-Herd auf. Nach topischer Kortikosteroidtherapie kam es nach etwa 3 Monaten zu einem zunehmenden Nachwachsen der Haare. Diese Fallberichte stellen erstmals einen ursächlichen Zusammenhang zwischen einer kutanen VZV-Infektion und permanenter vernarbender Alopezie sowie transitorischer Alopecia areata her. Lokalisierter Haarausfall sollte zu den kutanen Komplikationen der kutanen VZV-Infektion hinzugefügt werden.
    Type of Medium: Online Resource
    ISSN: 2296-5424 , 2296-536X
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2013
    detail.hit.zdb_id: 2736309-0
    detail.hit.zdb_id: 2741387-1
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