Search

The article describes the case of a four-year-old girl diagnosed with chronic muco-cutaneous candidiasis (CMCC) of the nails and mouth. Topics covered include the CMCC condition of the girl's mother and maternal aunts, the symptoms of the patient consistent with the CMCC diagnosis, fluconazole treatment administered to the patient and genetics of the familial forms of CMCC.

The article presents a case study of 81-year-old woman who was first observed due to the presence of mildly symptomatic nodular lesions of the face and limbs from six months. Her medical history revealed serous microcystic cystadenoma of the head of the pancreas removed five years before and her histological examination showed superficial and deep dermis. It highlights that the patient was diagnosed with pure cutaneous Rosai-Dorfman disease and prescribed dapsone for its treatment.

The article presents chronic granulomatous disease (CGD), a primary immunodeficiency caused by a nicotinamide-adenine-dinucleotde-phosphate (NADPH) oxidase enzyme defect and characterized by recurrent bacterial and fungal infections. It compares the skin lesions of CGD from idiopathic asceptic facial granuloma, a benign self-healing disease. Treatment for CGD included pharmacological prophylaxis and bone marrow transplantation while idiopathic asceptic facial granuloma has no treatment.

The article explores several cases of prepubertal longitudinal melanonychia, which includes the case of a 10-month-old infant who presented with a band-like pigmented lesion since birth and was later diagnosed with congenital melanocytic nevus and the case of an 8-year-old boy diagnosed with melanonychia due to recent acquired melanocytic nevus.

The article describes the case of a newborn infant born after 35 weeks of gestation by cesarean section with nodules and plaques of hard consistency in the trunk, and was diagnosed with calcinosis cutis universalis.

The article describes the case of a 10-month girl with the presence of an area of curly hair different from other hair since birth which was consistent with the diagnosis of epidermal nevus associated with wooly hair nevus.

A case report of a 5-month-old little boy showing demographic mastocytosis is presented.

A case report of a 30-year-old woman with symptomatic reddish lesions is presented during which she has a medical history of allergic rhynitis and physical diagnosis expressed papular lesions, blood-chemistry tests were normal in range and lymphocytic and eosinophilic infiltrate, and Kimura's disease.

The article describes the case of a 25-year-old girl who was diagnosed with transient lymphedema due to intense physical activity with the upper limbs.

The article presents a case of a 28-day-old infant who was first observed due to the presence of small raised neoformations of the nostrils. It mentions that baby was born via spontaneous natural delivery after a normal pregnancy and his physical examination showed dermatological milia of the face and increased evidence of the pilosebaceous follicles on the tip of the nose. It adds that the patient was diagnosed with Sebaceous hyperplasia of the nasal mucosa.

The article presents a case study of 10-year-old girl who was first observed due to the presence from two years on the flexor surface of the left forearm of asymptomatic lesions in linear distribution with centrifugal evolution. It mentions that her physical examination revealed lesions and based on clinical and dermoscopic findings, the patient was diagnosed with linear porokeratosis.

The article describes the case of zosteriform connective tissue nevus on the left buttock of a 13-year-old girl.

The article presents a case study of a 21 year old woman who was presented with a lesion in the thoraco-abdominal region whose clinical examination reveals diagnosis of superficial thrombophlebitis of thoraco-abdominal wall.

The article presents a case study of a13-year-old girl who was first observed in the Clinic of Pediatric Dermatology for presence of asymptomatic lesions on the torso and lower limbs who was diagnosed with lichen sclerosus.

The article discusses two case reports of pimple-like Mallorca acne in women. Topics include the medical history of the patients, details of the findings of their dermatological examinations, and the skin disorder's appearance on the lower neckline and shoulders characterized by the development of pustules and inflammation of hair follicles. It also said that it is not conclusive if Mallorca acne is caused by sunlight exposure.

The article presents a case study of a two-month-old little girl with a neoformation of the left frontal-parietal region who was taken under the diagnosis of congenital melanocytic nevus which showed hematoma within neuroid congenital melanocytic nevus.

The article describes the case of a 9-month-old newborn infant girl with concomitant mastocytosis and juvenile xanthogranuloma.

The article describes the case of a 15th-month-old newborn infant girl with a recurrent cutaneous neonatal herpes simplex (HS).

The article describes the case of a 27-year-old man diagnosed with acne induced by the use of corticosteroids.

The article describes the case of a two-year-old girl who was diagnosed with late onset acrodermatitis enteropathica.

The article describes the case of a 9-year old girl diagnosed with Phakomatosis pigmento-vascularis.

The article describes the case of a 6-year child with molluscum contagiosum superimposed on congenital melanocytic nevus.

The article describes the case of a 78-year old woman suffering from Schnitzler's syndrome (SS), an autoinflammatory disease, characterized by the presence of an Immunoglobulin G (IgG)- Immunoglobulin A (IgA) and acquired cuts laxa.

The article describes the case of a boy who was first observed at the age of 4 years for a lump on the medial surface of the left leg just below the knee, which the magnetic resonance imaging (MRI) revealed as a neoplasm composed of serpiginous structures.

The article describes the case of a 7-year-old girl who had recurrent acute urticaria with a lesion of the scalp.

The article describes the case of a 25-month-old child who has hospitalized for diabetes insipidus in oncohematology, which was first observed due to an exudative lesion of the right cheek.

The article describes the case of a 28 year old woman initially observed due to acrolocated and periorifical skin lesions. The administration of zinc sulfate three times daily resulted in a rapid remission of symptoms and led to a final diagnosis of acquired acrodermatitis enteropathica-like syndrome. It refers to zinc as an oligoelement necessary for protein synthesis whose absorption is poor in acrodermatitis enteropathica. It suggests the monitoring of zinc before starting parenteral nutrition and its possible supplementation.

The article describes the case of a 16 year old girl observed due to the presence of asymptomatic lesions of the face and limbs. A histological examination whose orthokeratotic hyperkeratosis leading to a final diagnosis of localized juvenile pityriasis rubra pilars. It is described as a heterogeneous group of diseases clinically characterized by inflammatory follicular keratosis, palmoplantar keratoderma and erythroderma. Its treatment is scarcely effective the usefulness of treatment with inhibitors of tumor necrosis factor has been supported lately.

The article describes the case of a four-month-old baby who was presented from a few weeks hair loss in the nuchal region and an itchy dermatitis. It was diagnosed as atopic dermatitis on nuchal salmon patch with hypertrichosis signs pointing to a physiological hair loss of the newborn. The salmon patch was hidden a hair present at birth and by an accompanying onset of atopic dermatitis extending outside the angioma. The hypertrichosis seemed to be related to several factors such as salmon patch, atopic dermatitis and the topical corticosteroid therapy.

The article describes the case of a 2-month old boy who was examined to have a rapidly growing 3-centimeter, round, skin colored nodule above the right heel. The nodule which was hard-elastic and movable on the deep layers, was removed under general anesthesia. The boy's final diagnosis is juvenile xanthogranuloma characterized with a single or multiple lesions. The single benign lesion in this case affects the dermis or subcutaneous tissue and has a xanthomized histiocytic infiltrate with Touton cells.

The article describes the case of a baby who was observed to have an upper right limb swelling after 5 days from birth. The swelling was manifested by a 3-centimeter, bluish, hemispherical and soft-elastic nodule with a 5-centimeter hypertrichotic area below the nodule. The angiomatous lesion reduced significantly after six months. The baby's final diagnosis is congenital hemangioma associated with smooth muscle hamartoma of the erector pili muscle which started to develop in the embryonic stage.

The article describes the case of a 42-day old boy who was observed to have a left frontal region swelling 6 hours after birth. Physical examination after a month revealed a 3-centimeter, soft-elastic and bluish plaque that is movable on the deep and superficial layers with three 2-millimeter nodules. The boy's final diagnosis is cephalhematoma caused by subperiosteal hematoma.