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Gastrointestinal Polyposis with Mucocutaneous Pigmentation (Peutz–Jeghers Syndrome)
New England Journal of Medicine, 1957THE syndrome of familial gastrointestinal polyposis associated with pigmentation of the skin and mucous membranes was described by Peutz1 in 1921, but only during the last six years has its compara...
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Bilateral diffuse uveal melanocytic proliferation with mucocutaneous pigmentation
Journal of Dermatology, 2015AbstractBilateral diffuse uveal melanocytic proliferation (BDUMP) is a rare paraneoplastic syndrome associated with extraocular malignancies. Extraocular pigmented lesions have been reported. We report that two patients with BDUMP presented with non‐ocular pigmented lesions.
Kazuhiro Kawai, Yuko Higashi
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Laugier–Hunziker syndrome: A rare cause of mucocutaneous pigmentation
British Journal of Oral and Maxillofacial Surgery, 2006An 80-year-old white woman presented with brown pigmentation on both sides of the buccal mucosa and lower lip and patchy freckling in her nails, which was diagnosed as Laugier-Hunziker syndrome.
T, Sabesan +2 more
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GASTROINTESTINAL POLYPOSIS WITH MUCOCUTANEOUS PIGMENTATION IN CHILDREN (PEUTZ-JEGHERS SYNDROME)
Pediatrics, 1961A case is reported in which a child had gastrointestinal polyposis associated with mucocutaneous pigmentations (the Peutz-Jeghers syndrome). He experienced severe recurrent abdominal pain caused by intermittent intussusception. Removal of the grossly palpable polyps from the small intestine and stomach controlled his symptoms.
Stickler Gunnar B
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Hemangiomas of the Small Intestine Associated With Mucocutaneous Pigmentation
Gastroenterology, 1960Summary A patient with multiple hemangiomas of the small intestine and mucocutaneous pigmentation is presented. The relationship of this entity to the Peutz-Jeghers syndrome is discussed.
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Idiopathic lenticular mucocutaneous pigmentation (laugier-hunziker syndrome): a report of a case
Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontics, 2003Laugier-Hunziker syndrome (LHS) is an acquired, benign, macular hyperpigmentation of the lips and oral mucosa, often associated with pigmentation of the nails. It is a rare disorder thought to be more common than the number of reported cases would suggest.
Tuula Salo, Maria Siponen
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Oral Surgery, Oral Medicine, and Oral Pathology, 1987
The complex of myxomas, spotty pigmentation, and endocrine overactivity is a recently recognized syndrome, transmitted as an autosomal dominant trait. The most serious component of the disorder is cardiac myxoma, which has caused the death of one fourth of the affected patients and serious disability in an equal number.
J Aidan Carney, Bruce A Lund
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The complex of myxomas, spotty pigmentation, and endocrine overactivity is a recently recognized syndrome, transmitted as an autosomal dominant trait. The most serious component of the disorder is cardiac myxoma, which has caused the death of one fourth of the affected patients and serious disability in an equal number.
J Aidan Carney, Bruce A Lund
exaly +3 more sources

