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  • 1
    Online Resource
    Online Resource
    Erythema infectiosumin children: A clinical study
    National Library of Serbia ; 2006
    In:  Medical review Vol. 59, No. 1-2 ( 2006), p. 5-10
    Details
    In: Medical review, National Library of Serbia, Vol. 59, No. 1-2 ( 2006), p. 5-10
    Abstract: Infektivni eritem je decija osipna bolest, koja se karakterise homogenim, jako izrazenim eritemom obraza i mrezastim osipom, lokalizovanim na ekstremitetima i trupu, bez hitnijeg poremecaja opsteg stanja. Izazivac je parvovirus B19. Javlja se periodicno, u zimskim i prolecnim mesecima. u vidu manjih epidemija. Dijagnoza se najcesce postavlja na osnovu karakteristicne klinicke slike i toka bolesti. Cilj naseg rada je bio da utvrdimo ucestalost i klinicke karakteristike infektivnog eritema kod obolele dece, koja su se javila na pregled na Odsek za dermatovenerologiju. Instituta za zdravstvenu zastitu dece i omladine u Novom Sadu, u periodu od 2000. do 2004. godine. Infektivni eritem je dijagnostikovan kod 0,23% dece. Prvi oboleli su se javili krajem 2001. godine. Od decembra 2001. do septembra 2002. godine dolazi do nagle pojave infektivnog eritema. Uocili smo znacajno cescu pojavu oboljenja tokom 2002. godine, a najveci broj obolelih je bio u maju i aprilu. Tokom 2003. i 2004. godine nismo dijagnostikovali infektivni eritem. Prosecan uzrast obolele dece je iznosio 7,38 godine. Obolelo je 56,41% devojcica i 43,58% decaka. Na svrab se zalilo 10,26% dece. Svega 5,12% dece je imalo opste simptome bolesti. Eritem obraza je imalo 89.74% dece. Mrezast osip na ekstremitetima je bio prisutan kod svih obolelih, a osip na trupu i ekstremitetima kod 7,68% dece. Limfadenopatiju je imalo 5,12% dece. Sva obolela deca imala su karakteristicnu klinicku sliku i dobrocudan tok bolesti. .
    Type of Medium: Online Resource
    ISSN: 0025-8105 , 1820-7383
    URL: Article
    DOI: 10.2298/MPNS0602005P
    Language: English
    Publisher: National Library of Serbia
    Publication Date: 2006
    detail.hit.zdb_id: 2381028-2
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  • 2
    Online Resource
    Online Resource
    Drug-related pityriasis rubra pilaris with acantholysis
    National Library of Serbia ; 2013
    In:  Military Medical and Pharmaceutical Journal of Serbia Vol. 70, No. 9 ( 2013), p. 871-873
    Details
    In: Military Medical and Pharmaceutical Journal of Serbia, National Library of Serbia, Vol. 70, No. 9 ( 2013), p. 871-873
    Abstract: Uvod. Akantoliza je retko prikazivana histoloska karakteristika Pityriasis rubra pilaris (PRP) ciji znacaj u diferencijalnoj dijagnozi prema psorijazi je nedavno prepoznat. Prikaz bolesnika. Prikazali smo odraslog bolesnika sa eritemoskvamoznom erupcijom po glavi i gornjem delu trupa pracenom svrabom koji je poceo nedelju dana nakon uvodjenja simvastatina. Tokom mesec dana razvila se eritrodermija sa ostrvcima postedjene koze. Histoloski nalaz suprabazalne akantolize sa naizmenicnim zonama hiperkeratoze i parakeratoze u epidermisu i inflamatornog infiltrata u dermisu potvrdio je klinicku dijagnozu klasicnog adultnog oblika PRP. Terapija acitretinom dovela je do izlecenja koznih promena. Epikutani patch test sa simvastatinom bio je negativan, scratch test bio je pozitivan, a test ekspozicije nije uradjen jer je procenjeno da u tom momentu nosi veliki rizik. Epizoda PRP pokrenuta lekom je najverovatnije objasnjenje za vremensku povezanost koznih promena sa pocetkom uzimanja simvastatina. Zakljucak. U lecenju retkih zapaljenskih oboljenja koze treba pazljivo da tumacimo znacaj kako dijagnostickih parametara, tako i mogucih spoljasnjih uticaja na tok oboljenja.
    Type of Medium: Online Resource
    ISSN: 0042-8450 , 2406-0720
    URL: Article
    DOI: 10.2298/VSP1309871G
    Language: English
    Publisher: National Library of Serbia
    Publication Date: 2013
    detail.hit.zdb_id: 2169819-3
    SSG: 15,3
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  • 3
    Online Resource
    Online Resource
    Tick-borne lymphadenopathy acquired in Serbia: Report of two cases
    National Library of Serbia ; 2018
    In:  Military Medical and Pharmaceutical Journal of Serbia Vol. 75, No. 11 ( 2018), p. 1134-1137
    Details
    In: Military Medical and Pharmaceutical Journal of Serbia, National Library of Serbia, Vol. 75, No. 11 ( 2018), p. 1134-1137
    Abstract: nema
    Type of Medium: Online Resource
    ISSN: 0042-8450 , 2406-0720
    URL: Article
    DOI: 10.2298/VSP161223035G
    Language: English
    Publisher: National Library of Serbia
    Publication Date: 2018
    detail.hit.zdb_id: 2169819-3
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  • 4
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    Online Resource
    Infantile hemangioma of the upper eyelid in one very and in two extremely preterm infants
    National Library of Serbia ; 2023
    In:  Military Medical and Pharmaceutical Journal of Serbia , No. 00 ( 2023), p. 38-38
    Details
    In: Military Medical and Pharmaceutical Journal of Serbia, National Library of Serbia, , No. 00 ( 2023), p. 38-38
    Abstract: Introduction. Infantile hemangiomas (IHs) are the most common vascular tumors of infancy. Their frequency increases with decreasing gestational age. Periorbital IHs (PIHs), although rare, have a high complication rate, with a substantial risk of impaired vision and aesthetic consequences. Thus, they are considered high-risk IHs and require treatment. In the available literature there is little information about the treatment of IHs in very and extremely preterm infants. Case report. We present three male infants (one very and two extremely prematurely born) with PIHs involving the upper eyelid. In all three cases IHs were solitary but with different subtypes according to soft-tissue depth (superficial; combined; deep). In none of the cases no additional congenital anomalies were found. An individualized approach to the management of each patient was applied. All infants were treated with oral propranolol, with careful monitoring for potential side effects and adjustment of treatment accordingly. Introduction of oral propranolol was carried out in a hospital setting, with a gradual increase of the drug dose, until the target dose is reached. Conclusion. In the case of PIH, an ophthalmologist is an inevitable part of the medical team. Very and extremely preterm infants are already under the supervision of an ophthalmologist due to mandatory screening for retinopathy of prematurity, but if they also have PIHs, monitoring must be particularly detailed and long-lasting.
    Type of Medium: Online Resource
    ISSN: 0042-8450 , 2406-0720
    URL: Article
    DOI: 10.2298/VSP240402038Z
    Language: English
    Publisher: National Library of Serbia
    Publication Date: 2023
    detail.hit.zdb_id: 2169819-3
    SSG: 15,3
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  • 5
    Online Resource
    Online Resource
    Dermoscopy Of The Month: Dermoscopic Finding of Pigment Network in Lesions of Eruptive Syringoma
    Walter de Gruyter GmbH ; 2018
    In:  Serbian Journal of Dermatology and Venereology Vol. 10, No. 1 ( 2018-03-01), p. 25-28
    Details
    In: Serbian Journal of Dermatology and Venereology, Walter de Gruyter GmbH, Vol. 10, No. 1 ( 2018-03-01), p. 25-28
    Abstract: Syringoma is a benign adnexal tumor derived from intraepidermal eccrine ducts. The usual presentation of syringoma is a small smooth skin-colored, yellowish or brownish papule with flattened or rounded top. Eruptive syringoma is a rarely reported form, where lesions are numerous and occur in successive crops. A case of a 57-year-old Caucasian male with a twenty four-year history of multiple asymptomatic, erythematous and brownish papules, predominantly over the anterior aspect of the trunk is presented. All lesions appeared after prolonged sun exposures within a few days and persisted without further changes afterwards. Contact non-polarized dermoscopy showed a fine light brown, regular pigment network on a light pink background, being the same in all lesions. History of the disease, clinical finding and dermoscopy were inconclusive, and biopsy was performed. Histopathology revealed signs of syringoma. Dermoscopic finding was thought to be intriguing and therefore is discussed in this paper.
    Type of Medium: Online Resource
    ISSN: 2406-0631 , 1821-0902
    URL: Article
    DOI: 10.2478/sjdv-2018-0005
    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2018
    detail.hit.zdb_id: 2862612-6
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  • 6
    Online Resource
    Online Resource
    National Guidelines for the Treatment of Atopic Dermatitis
    Walter de Gruyter GmbH ; 2016
    In:  Serbian Journal of Dermatology and Venereology Vol. 8, No. 3 ( 2016-9-1), p. 129-153
    Details
    In: Serbian Journal of Dermatology and Venereology, Walter de Gruyter GmbH, Vol. 8, No. 3 ( 2016-9-1), p. 129-153
    Type of Medium: Online Resource
    ISSN: 2406-0631 , 1821-0902
    URL: Article
    DOI: 10.1515/sjdv-2016-0012
    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2016
    detail.hit.zdb_id: 2862612-6
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  • 7
    Online Resource
    Online Resource
    Unilateral Laterothoracic Exanthem – Asymmetric Periflexural Exanthem of Childhood – a Case Report and Literature Review
    Walter de Gruyter GmbH ; 2017
    In:  Serbian Journal of Dermatology and Venereology Vol. 9, No. 2 ( 2017-6-27), p. 49-52
    Details
    In: Serbian Journal of Dermatology and Venereology, Walter de Gruyter GmbH, Vol. 9, No. 2 ( 2017-6-27), p. 49-52
    Abstract: Unilateral laterothoracic exanthem (ULE), or asymmetric periflexural exanthem of childhood (APEC), is an uncommon skin eruption that usually occurs in childhood, with unilateral distribution and self limiting course. The etiology of ULE is unknown, but viral cause is suspected. We report a case of ULE in a 4-year-old girl, that was associated with parvo virus B19 infection, and a brief selected literature review. The patient presented with unilateral maculopapular rash on the left side of the body which was asymptomatic and resolved spontaneously within 5 weeks. The clinical diagnosis of ULE may be precise, ruling out a broad spectrum of differential diagnosis, and prevent unnecessary examinations, whereas the patient is informed about the benign self-limiting nature of ULE.
    Type of Medium: Online Resource
    ISSN: 2406-0631 , 1821-0902
    URL: Article
    DOI: 10.1515/sjdv-2017-0007
    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2017
    detail.hit.zdb_id: 2862612-6
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  • 8
    Online Resource
    Online Resource
    Superficial Genital Infantile Hemangiomas
    Walter de Gruyter GmbH ; 2019
    In:  Serbian Journal of Dermatology and Venereology Vol. 11, No. 1 ( 2019-03-01), p. 19-24
    Details
    In: Serbian Journal of Dermatology and Venereology, Walter de Gruyter GmbH, Vol. 11, No. 1 ( 2019-03-01), p. 19-24
    Abstract: Introduction. Superficial infantile hemangiomas (IH) are rarely localized in the genital region. Case Report. We present 8 infants with IHs in the genital region (3 boys and 5 girls). Our patients had only superficial IHs, their internal organs were not affected and there were no associated anomalies. In the boys, IHs were localized on the scrotum and the foreskin in 2 cases and 1 case, respectively. In the girls, IHs were on the labia majora and near the vaginal introitus. None of the IHs showed any IH-related complications. No therapy for IHs was administered in any of the presented infants, either because IHs were small and non-aggressive, or because their parents rejected the proposed therapy. Conclusion. Genital IHs have increased tendency for ulceration, so thorough examination and follow-up are of outmost importance. If therapy is indicated, oral propranolol is the treatment of choice for genital IHs.
    Type of Medium: Online Resource
    ISSN: 2406-0631 , 1821-0902
    URL: Article
    DOI: 10.2478/sjdv-2019-0003
    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2019
    detail.hit.zdb_id: 2862612-6
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  • 9
    Online Resource
    Online Resource
    Secondary Tumor Arising in a Nevus Sebaceous
    Walter de Gruyter GmbH ; 2020
    In:  Serbian Journal of Dermatology and Venereology Vol. 12, No. 4 ( 2020-12-01), p. 147-151
    Details
    In: Serbian Journal of Dermatology and Venereology, Walter de Gruyter GmbH, Vol. 12, No. 4 ( 2020-12-01), p. 147-151
    Abstract: Introduction. Nevus sebaceous is a rare congenital hamartoma, composed of epidermis, sebaceous glands, sweat glands and hair follicles. It is possible to develop secondary tumors in the area of nevus sebaceous during the lifetime, most often after puberty. Secondary lesions are most often benign, while malignant lesions may occur but significantly less frequently. Case report. We present the case of a 21-year-old patient who came for an examination due to the appearance of a nodule in the area of a yellowish lesion on the head. The yellowish lesion was present since birth, and the nodule appeared about a year before. The dermoscopic examination of the lesion was nonspecific. The final diagnosis of eccrine poroma as a secondary lesion in nevus sebaceous was made by pathohisto-logical analysis. Conclusion. Every secondary tumor in nevus sebaceous deserves full attention, with either close follow up, or excision with pathohistological analysis.
    Type of Medium: Online Resource
    ISSN: 2406-0631 , 1821-0902
    URL: Article
    DOI: 10.2478/sjdv-2020-0018
    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2020
    detail.hit.zdb_id: 2862612-6
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  • 10
    Online Resource
    Online Resource
    Bullous aplasia cutis congenita: A report of two cases and brief review of the selected literature
    National Library of Serbia ; 2019
    In:  Military Medical and Pharmaceutical Journal of Serbia Vol. 76, No. 3 ( 2019), p. 345-348
    Details
    In: Military Medical and Pharmaceutical Journal of Serbia, National Library of Serbia, Vol. 76, No. 3 ( 2019), p. 345-348
    Abstract: nema
    Type of Medium: Online Resource
    ISSN: 0042-8450 , 2406-0720
    URL: Article
    DOI: 10.2298/VSP170201076P
    Language: English
    Publisher: National Library of Serbia
    Publication Date: 2019
    detail.hit.zdb_id: 2169819-3
    SSG: 15,3
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