Concurrent congenital fibrolipomatous hamartoma and congenital nevus of infancy: A syndromic or chance association

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منابع مشابه

Precalcaneal congenital fibrolipomatous hamartoma.

, 1202–1203 © 2005 The International Society of Dermatology 1202 The patients are four unrelated children, one boy and three girls, aged between 3 and 7 months. All the patients were born at term, had normal postnatal development, and were in good general health. Each child presented from birth with a single plantar nodule, between 0.5 and 1.5 cm in diameter, bilaterally and symmetrically local...

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Precalcaneal congenital fibrolipomatous hamartoma.

Precalcaneal congenital fibrolipomatous hamartomas (PCFHs) are characterized clinically by the presence of unilateral or bilateral, asymptomatic nodules in the medial precalcaneal plantar region of the heel. They are skin colored and usually painless nodules. In most patients, the lesions appear within the first few months of life, but they may also be present at birth. Generally PCFHs are beni...

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Nasal congenital fibrolipomatous hamartoma in a premature infant.

Hamartomas are tumor-like lesions composed of tissue elements normally found at the site where they are located, but which grow in a disorganized manner. They generally occur at birth or soon after, although presentations during adult life have been reported. Hamartomas of the head and neck are very rare. The exact mechanisms behind the development of hamartomas remain unknown; however, their b...

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Two Cases of Giant Congenital Cutaneous Hamartoma: Nevus Sebaceus of Jadassohn and Congenital Melanocytic Nevus

During the normal development of skin, pluripotential cells give rise to keratinocytes, sebaceus glands, hair follicles, apocrine glands and eccrine glands. A hamartoma, or an abnormal mixture of a tissue’s normal components, results from an error in development, among which some show malignant potential. We report two Chinese cases of giant congenital cutaneous hamartoma, a nevus sebaceus of J...

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Bilateral congenital nevus of Ota in association with Mongolian spot

A 24-year-old woman presented with asymptomatic hyperpigmented bilateral patches on her temples, eyelids and forehead since birth. Furthermore, the patient had a congenital grey patch, compatible with Mongolian spot, on her buttock. She had no vascular or other cutaneous lesion. Histopathologic examination revealed bipolar dendritic melanocytes dispersed in a ribbon-like pattern between the col...

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ژورنال

عنوان ژورنال: Journal of Indian Association of Pediatric Surgeons

سال: 2018

ISSN: 0971-9261

DOI: 10.4103/jiaps.jiaps_163_17