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Neonatal Skin (neonatal + skin)
Selected AbstractsMammary Skin Tag in a 2-Year-Old Girl: A Long-Lasting Adnexal Polyp Of Neonatal Skin?PEDIATRIC DERMATOLOGY, Issue 5 2009ANA LUCAS COSTA M.D. Clinical and histological features were consistent with an adnexal polyp of neonatal skin observed beyond the neonatal period. [source] Skin care for preterm and term neonatesCLINICAL & EXPERIMENTAL DERMATOLOGY, Issue 8 2009F. S. Afsar Summary Neonatal skin experiences a progressive adaptation to the extrauterine environment during which special care is needed. The immaturity of the epidermal barrier in the neonatal period may cause dry skin, vulnerability to trauma, rapid onset of microbial colonization and percutaneous drug toxicity. This article reviews the practical implications for hygiene, bathing practices, skin integrity, emollient use, infection control and exposure to percutaneous toxic agents in preterm and term infants. [source] Iris as a recipient tissue for pigment cells: Organized in vivo differentiation of melanocytes and pigmented epithelium derived from embryonic stem cells in vitroDEVELOPMENTAL DYNAMICS, Issue 9 2008Hitomi Aoki Abstract Regenerative transplantation of embryonic stem (ES) cell-derived melanocytes into adult tissues, especially skin that includes hair follicles or the hair follicle itself, generally not possible, whereas that of ES cell-derived pigmented epithelium was reported previously. We investigated the in vivo differentiation of these two pigment cell types derived from ES cells after their transfer into the iris. Melanocytes derived from ES cells efficiently integrated into the iris and expanded to fill the stromal layer of the iris, like those prepared from neonatal skin. Transplanted pigmented epithelium from either ES cells or the neonatal eye was also found to be integrated into the iris. Both types of these regenerated pigment cells showed the correct morphology. Regenerated pigment epithelium expressed its functional marker. Functional blocking of signals required for melanocyte development abolished the differentiation of transplanted melanocytes. These results indicate successful in vivo regenerative transfer of pigment cells induced from ES cells in vitro. Developmental Dynamics 237:2394,2404, 2008. © 2008 Wiley-Liss, Inc. [source] Predominant formation of heavily pigmented dermal melanocytomas resembling ,animal-type' melanomas in hepatocyte growth factor (C57BL/6 × C3H)F1 mice following neonatal UV irradiationJOURNAL OF CUTANEOUS PATHOLOGY, Issue 9 2007Scott R. Florell Background:, Transgenic mice expressing hepatocyte growth factor (HGF) develop cutaneous melanocytic tumors following neonatal UV exposure. Here, we examined the histologic spectrum of UV-induced melanocytic tumors in HGF mice on a pigmented (C57BL/6 × C3H/HeN)F1 background. Methods:, Neonatally irradiated (4000 J/m2) mice were monitored for 43 weeks, and 31/34 (91%) animals developed a total of 163 melanocytic tumors. Results:, Of 54 primary tumors analyzed, most (49/54, 91%) demonstrated exclusively dermal collections of epithelioid cells with voluminous densely pigmented cytoplasm. Seven of these also demonstrated a population of spindled cells with mitoses. Several (3/54, 6%) tumors exhibited a junctional component with melanocytes present in the epidermis. Staining with PEP8 confirmed the presence of interfollicular melanocytes at the dermal-epidermal junction in neonatal skin. Conclusions:, In contrast to HGF animals on an albino (FVB) background, HGF animals on the pigmented (C57BL/6 × C3H/HeN)F1 background do not develop classic radial growth phase melanoma but rather predominantly develop dermal melanocytomas resembling the ,animal-type' melanoma occasionally seen in humans. These results demonstrate the influence of genetic background on histologic pattern of UV-induced melanomas in mice. [source] Mammary Skin Tag in a 2-Year-Old Girl: A Long-Lasting Adnexal Polyp Of Neonatal Skin?PEDIATRIC DERMATOLOGY, Issue 5 2009ANA LUCAS COSTA M.D. Clinical and histological features were consistent with an adnexal polyp of neonatal skin observed beyond the neonatal period. [source] Neonatal pemphigus vulgaris with extensive mucocutaneous lesions from a mother with oral pemphigus vulgarisBRITISH JOURNAL OF DERMATOLOGY, Issue 4 2002A. Campo-Voegeli Summary The clinical phenotype of pemphigus is well explained by the combination of desmoglein (Dsg) 1 and Dsg3 distribution pattern and antiDsg autoantibody profile (Dsg compensation theory). It has been reported that neonatal skin has a similar Dsg distribution pattern to adult mucosal epithelia. We describe a newborn girl with mucocutaneous pemphigus vulgaris (PV) from a mother with mucosal dominant PV. The mother had had painful oral erosions for at least 7 months. Histopathological examination and direct and indirect immunofluorescence studies confirmed the diagnosis of PV and neonatal PV in the mother and daughter, respectively. The mother had a high titre of anti-Dsg3 IgG and a low titre of antiDsg1 IgG, while the neonate had only a high titre of anti-Dsg3 IgG, but no detectable antiDsg1 IgG. AntiDsg3 IgG, which caused the oral dominant phenotype in the mother, induced extensive oral as well as cutaneous lesions in the neonate. Our case provides clinical evidence for the Dsg compensation theory in neonatal PV. [source] Physiological skin conditions of preterm and term neonatesCLINICAL & EXPERIMENTAL DERMATOLOGY, Issue 4 2010F. S. Afsar Summary Skin problems in children during the first few weeks of life can raise concern, even for experienced neonatologists and paediatric dermatologists. The skin of preterm and term newborn babies has distinct differences from juvenile and adult skin. An understanding of the nature of neonatal skin, the physiological and nonphysiological skin conditions of preterm and term neonates, and skin care are essential in paediatric practice. This article discusses the nature of the neonatal skin and its physiological phenomena. [source] | ||||||||||