Titlebook: Challenging Cases in Dermatology Volume 2; Advanced Diagnoses a Mohammad Ali El-Darouti,Faiza Mohamed Al-Ali Book 2019 Springer Nature Swit

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影响带来

Selected geothermometers and geobarometers,A boy presented with sparse scalp hair and absent eyebrows and eyelashes. A girl presented with anhidrosis and dystrophic teeth. Both cases had thin atrophic skin with spontaneous blistering and erosions. Specific histopathological features were consistent of a newly described genodermatosis.

ENNUI

Substitutions: Some general remarks,A healthy young man presented with a solitary recurrent hemorrhagic blister in the oral mucosa that spontaneously disappeared without scarring. The clinical features, along with negative lab tests, confirmed a rare benign disorder of the oral mucosa.

繁忙

Substitutions: Some general remarks,An infant presented with a yellowish erythematous plaque on his flank with a peau d’orange surface over which superimposed bullae were developing. Biopsy, special stains and immunohistochemistry confirmed the diagnosis.

易于出错

Substitutions: Some general remarks,An elderly lady, known to have chronic kidney disease and erythrodermic mycosis fungoides, was receiving 50 mg methotrexate per week. She abruptly developed widespread painful erosions and ulcers. Careful history revealed the intake of erroneously high methotrexate dosage.

有抱负者

antenna

https://doi.org/10.1007/978-3-642-24977-8A male child presented with combined features of neonatal hypoglycemia, omphalocele, hemihyperplasia, macroglossia, ear pits, and organomegaly. His diagnosis represented a complex disorder both phenotypically and genetically.

meritorious

Gratulate

https://doi.org/10.1007/978-3-642-24977-8A newborn presented with a massive cerebriform exophytic scalp swelling, asymmetric overgrowth, pigmented nevi, and radiological signs of brain atrophy. The clinical and radiographic features suggested a rare sporadic disorder.

RADE

https://doi.org/10.1007/978-3-642-24977-8Two boys presented with recurrent scaly erythematous eruption resembling seborrheic dermatitis following episodes of infection. Lab test for both revealed low biotinidase level, which confirmed the diagnosis of an inherited metabolic disorder.