[Dr.Anisimova]

Papulovesicular eruption located on the face and extremities in a child
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Hydroa vacciniforme (HV) is a rare, acquired photodermatosis of unknown etiology, which predominantly affects children. It is characterized by the occurrence of vesicles on light-exposed areas, especially the malar areas, bridge of the nose, lips, ears, and the dorsa of the hands and forearms, a few hours after sun exposure. The vesicles crust and heal over a period of 1-6 weeks, leaving varioliform scars

Multiple congenital vascular lesions in a child
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Propranolol vs Corticosteroids for Infantile Hemangiomas[Ссылки доступны только зарегистрированным пользователям ]
Conclusions* Propranolol therapy was more clinically effective and more cost-effective than oral corticosteroids in treating IHs. It also resulted in fewer surgical interventions and demonstrated better tolerance, with minimal adverse effects, compared with oral corticosteroids. Therefore, propranolol should be considered a first-line agent given its safety and efficacy in the treatment of IHs.

Clonality of Staphylococcus aureus Colonization over Time in Attendees of a Camp for Children with Chronic Dermatoses
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Taken together, our findings demonstrate that colonization with S.*aureus is frequent in children and young adults with CD, but significant variability exists in colonizing strains over time. In these individuals, frequent contact with each other and with persons without dermatoses in a supervised camp setting did not appear to be related to adverse clinical outcomes.

Neonatal Linear Immunoglobulin A Bullous Dermatosis: A Rare Presentation
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Frontal Congenital Lipoma
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Infant epidermal skin-physiology: Adaptation after birth
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Necrolytic Acral Erythema in an Adolescent
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Terra Firma-Forme Dermatosis: A Retrospective Review of 31 Patients
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TFFD is one of the dirtlike dermatoses (4), along with dermatitis neglecta, confluent and reticulated papillomatosis, and acanthosis nigricans. The differential diagnosis of TFFD should also include the “dirty neck syndrome” of atopic dermatitis (5), which is more common in adults, is macular, and cannot be removed with alcohol swabbing. Because TFFD is readily identified and treated, biopsies have rarely been taken, limiting the availability of histopathological analyses that might shed light on why this condition occurs. In addition to the sparse histopathologic information, clinical data regarding TFFD is limited in the literature, which previously contained no large series.
It is important for pediatricians and dermatologists to recognize TFFD. In addition to the many patients who experienced painful attempts at cleansing (by parents or patients themselves), more than one-fifth of the cases here (and many in the literature) had unnecessary prescriptions or blood tests. Recognizing and treating this condition can be gratifying for physicians, who can provide almost instant relief to their sometimes stunned patients.

Anaplastic Large Cell Lymphoma: An Unusual Presentation in a 7-Year-Old Girl
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An Unusual Presentation of Idiopathic Basal Cell Carcinoma in an 8-Year-Old Child
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Bilateral Milia En Plaque in a 6-Year-Old Chinese Boy
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Malakoplakia
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Malakoplakia is a rare, chronic disease with pleomorphic presentation. It occurs most frequently in immunocompromised patients. It is believed that this entity represents an unusual response to bacterial infection in which macrophages fail to phagocytose them properly. It involves many organs, particularly the urinary and gastrointestinal tracts. It is uncommon on the skin and less common in children. The diagnosis is usually based on histopathologic findings.

Poikiloderma with Neutropenia: Report of Three Cases Including One with Calcinosis Cutis
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