نتایج جستجو برای: hamartomatous

تعداد نتایج: 561  

2001
Alice Rebelo de Matos Borges dos Reis Frederico Becker Ribeiro Regina Schultz

Congenital cystic adenomatoid malformation (CCAM) is an hamartomatous congenital pulmonary airway malformation with incidence ranging between 1:10,000 and 1:35,000 newborns. Currently CCAM is classified into five groups according to clinical and pathological features. The clinical outcome varies depending on the subtype and the extent of involvement. The authors report the case of a premature m...

2015
George Abraham Sateesh R. Prakash

Ganglioneuromas (GNs) are hamartomatous tumors derived from the autonomic nervous system. It is rare to encounter GN in the gastrointestinal tract. Patients with these tumors usually present with abdominal pain, constipation, ileus, weight loss, or even bleeding. GNs are categorized into three different morphological subtypes, namely, polypoid GN, ganglioneuromatous polyposis, and diffuse gangl...

Journal: :Acta dermato-venereologica 1999
D H Kim C W Kim T Y Kim

Sir, Becker's naevus or Becker's melanosis is a relatively common disorder, which appears as a hyperpigmented, hypertrichotic patch located mainly on the trunk (1). Becker's naevus has been associated with various soft tissue and bony structural anomalies, such as hypoplasia of the ipsilateral breast, pectoralis major muscle, leg, arm and contralateral breast, spina bi®da, and pectus carinatum ...

Journal: :Dermatology online journal 2008
Santos Patrícia Neto Cláudia Machado Susana Lobo Inês Soares José Selores Manuela

Pigmented spots in the skin and mucosa (lentigines) can be found in various diseases called familial lentiginosis syndromes; Peutz-Jeghers syndrome (PJS) is one of them. It is characterized by the association of mucocutaneous melanin pigmentation and hamartomatous gastrointestinal polyps. Patients with PJS are at increased risk of intussusception and cancer development (gastrointestinal and non...

2007

Case report: Congenital disfiguring malformations are rare and usually have a multifactorial aetiology. Here we report on the ocular manifestations seen in a patient with Proteus syndrome. The retina showed retinal dysgenesia, retinal pigmentary abnormalities and optic nerve hypoplasia. Other abnormalities included strabismus and high myopia. Discussion: Proteus syndrome is a complex hamartomat...

2016
Samira Yarak Taila Yuri Siqueira Machado Marilia Marufuji Ogawa Mirian Luzia da Silva Almeida Milvia Maria Simões e Silva Enokihara Adriana Maria Porro

Verrucous epidermal nevi are hamartomatous lesions of the epidermis that, unlike other epidermal nevi (such as sebaceous nevus or nevus comedonicus), are rarely associated with malignant neoplasms. The majority of squamous cell carcinoma develop in linear or multiple epidermal nevus and rarely in solitary epidermal nevus. In general, the prognosis is favorable. We report a case of well-differen...

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