Publications by authors named "Shinkuma S"

Background: Epidermal growth factor receptor inhibitors (EGFRIs) reduce β-defensin 3 (BD3) from keratinocytes stimulated by S. epidermidis, potentially leading to the development of acneiform rashes in patients undergoing EGFRIs treatment. However, the mechanism through which S.

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The histopathologic diagnosis of poorly differentiated cutaneous angiosarcoma can be challenging. We report a case of cutaneous epithelioid angiosarcoma with numerous multinucleated giant cells (MGCs) developing pulmonary metastasis. A 79-year-old man presented with a red-purple plaque on the scalp.

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Nevus lipomatosus cutaneous superficialis is a rare, benign hamartoma characterized by mature adipocyte proliferation in the dermis. It is frequently difficult to distinguish clinically from soft tissue tumors, including lipoma, neurofibroma, venous malformation, and angiolipoma. Notably, the classical form, which shows multiple and sometimes enlarged nodules, is difficult to differentiate from liposarcoma based on clinical examination, computed tomography, and magnetic resonance imaging findings.

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  • Infancy associated eosinophilic pustular folliculitis (I-EPF) is a variant of eosinophilic pustular folliculitis that occurs in children and shows distinct clinical and histological differences from classic EPF.
  • A study of two patients with I-EPF treated with topical indomethacin revealed unique patterns of eosinophilic infiltration compared to classic EPF, specifically less perifollicular and more perivascular infiltration.
  • Immunohistochemical analysis indicated that both I-EPF and classic EPF have CD4-dominant T cells, but classic EPF has significantly more CD68-positive cells; HPGDS-positive cells that promote eosinophil activity were also
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  • Epidermolytic ichthyosis (EI) is a genetic skin disorder that causes severe skin dryness and scaling due to mutations in KRT1/KRT10, with limited understanding of underlying cytokine profiles and treatment options.
  • This study aimed to identify potential biomarkers and therapeutic targets by analyzing cytokine levels in serum and skin samples from patients with EI, focusing on the effects of mutant KRT1.
  • Results revealed significantly elevated levels of IL-18 in EI patients, correlating with the severity of their condition, and suggested that mutant keratin may activate the NLRP3 inflammasome, contributing to the disease pathology.
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An autosomal recessive disease is caused by biallelic loss-of-function mutations. However, when more than two disease-causing variants are found in a patient's gene, it is challenging to determine which two of the variants are responsible for the disease phenotype. Here, to decipher the pathogenic variants by precise haplotyping, we applied nanopore Cas9-targeted sequencing (nCATS) to three truncation COL7A1 variants detected in a patient with recessive dystrophic epidermolysis bullosa (EB).

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Background: The live attenuated varicella-zoster virus (VZV) vaccine is used for the prevention of chickenpox and herpes zoster; however, there have been few studies on the immunogenicity of intradermal vaccination.

Objective: To compare the immunogenicity between subcutaneous and intradermal VZV vaccination.

Methods: Thirty healthy participants aged 50-75 who developed erythema less than 10 mm in diameter in VZV skin test were examined.

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Epidermolysis bullosa (EB) is a group of inherited skin and mucosal fragility disorders resulting from mutations in genes encoding basement membrane zone (BMZ) components or proteins that maintain the integrity of BMZ and adjacent keratinocytes. More than 30 years have passed since the first causative gene for EB was identified, and over 40 genes are now known to be responsible for the protean collection of mechanobullous diseases included under the umbrella term of EB. Through the elucidation of disease mechanisms using human skin samples, animal models, and cultured cells, we have now reached the stage of developing more effective therapeutics for EB.

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Background: Drug-induced hypersensitivity syndrome/drug reaction with eosinophilia and systemic symptoms (DIHS/DRESS) is a severe adverse drug reaction commonly associated with the reactivation of human herpesvirus 6 (HHV-6). There are currently no adequate biomarkers for the early diagnosis and detection of DIHS/DRESS. Notably, OX40 (CD134) has an important role in allergic inflammation and functions as a cellular receptor for HHV-6 entry.

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Hemidesmosomes (HDs) are adhesion complexes that promote epithelial-stromal attachment in stratified and complex epithelia, including the epidermis. In various biological processes, such as differentiation and migration of epidermal keratinocytes during wound healing or carcinoma invasion, quick assembly and disassembly of HDs are prerequisites. In this study, we show that inhibition of Wnt/β-catenin signaling disturbs HD organization in keratinocytes.

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Background: Stevens-Johnson syndrome (SJS)/toxic epidermal necrolysis (TEN) is a life-threatening cutaneous adverse drug reaction (cADR). Distinguishing SJS/TEN from nonsevere cADRs is difficult, especially in the early stages of the disease.

Objective: To overcome this limitation, we developed a computer-aided diagnosis system for the early diagnosis of SJS/TEN, powered by a deep convolutional neural network (DCNN).

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  • Acral persistent papular mucinosis is a rare form of lichen myxedematosus, characterized by small, whitish papules on the hands, as seen in a case study of a 41-year-old woman with a 5-year history of the condition.
  • Histopathological examination showed distinct findings, including sparse collagen in the dermis and positive Alcian blue staining, confirming the diagnosis.
  • Despite prior indications that tranilast may help manage this condition, the patient did not show improvement after two months of treatment, highlighting the need for further research on its effectiveness.
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  • Recent advancements in genetic engineering have enabled gene therapy to be used not only for congenital diseases but also for acquired conditions like cancer.
  • Several gene therapeutic agents for immune disorders, hemophilia, and skin diseases have been approved in the U.S. and Europe, indicating progress in this field.
  • The review discusses various gene transfer techniques and their application in treating skin diseases, highlighting the complexity and evolving status of gene therapy in dermatology.
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