ReviewFamilial cancer2011
The differential diagnosis of familial lentiginosis syndromes.
Review in Familial cancer, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
18 citing papers in PubMed.
- Co-Occurrence of Agminated Lentigines, Café-Au-Lait Macules, and Vitiligo: A Case Report and Literature Review.Clinical case reports · 2026Article
- Case Report: Hyperthyroidism in a patient with spotty skin pigmentation and atrial myxoma (Carney complex): coincidence, association or cause?Frontiers in cardiovascular medicine · 2026Article
- Peutz-Jeghers syndrome: Skin manifestations and endocrine anomalies (Review).Experimental and therapeutic medicine · 2021Review
- Review
- LEPOARD syndrome: A report of a case with a novel PTPN11 mutation.JAAD case reports · 2021Article
- LEOPARD Syndrome withJournal of pediatric genetics · 2020Article
- Pigmented pruritic papules in a middle-age man.JAAD case reports · 2020Article
- [Pigmented macules as possible early signs of genetic syndromes].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2019Review
- Patient with confirmed LEOPARD syndrome developing multiple melanoma.Dermatology practical & conceptual · 2018Article
- Hereditary syndromes predisposing to endocrine tumors and their skin manifestations.Reviews in endocrine & metabolic disorders · 2016Review
- Lentiginoses in polycythemia vera patient: Is there a role for JAK2 (V617F) mutation?JAK-STAT · 2015Article
- An aroma of complexity: how the unique genetics of aromatase (CYP19A1) explain diverse phenotypes from hens and hyenas to human gynecomastia, and testicular and other tumors.The Journal of clinical endocrinology and metabolism · 2013Article
- Paraneoplastic disseminated lentigines heralding aggressive Langerhans cell sarcoma.Annals of hematology · 2013Article
- Sudden Death in a Patient with Carney's Complex.Anesthesiology and pain medicine · 2013Article
- [Peutz-Jeghers syndrome : not only a polyposis!].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2012Article
- Large-cell calcifying Sertoli cell tumors of the testes in pediatrics.Current opinion in pediatrics · 2012Review
- LKB1/ STK11, Peutz-Jeghers syndrome and cancer. Introduction.Familial cancer · 2011Article
- Voriconazole-induced lentiginosis in a child: a phototoxicity warning sign.Anais brasileiros de dermatologiaArticle
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
Cutaneous markers of systemic disease are vital for clinicians to recognize. This chapter outlines familial lentiginosis syndromes that include Peutz-Jeghers syndrome, Carney Complex, the PTEN hamartomatous syndromes, and LEOPARD/Noonan syndrome. The inheritance of these syndromes is autosomal dominant; they also share characteristic skin findings that offer a clue to their recognition and treatment. We will discuss the clinical presentation of these disorders, with a focus on the dermatological manifestations, and will provide an update on the molecular mechanisms involved. Recognition of cutaneous markers associated with these rare familial cancer syndromes provides the opportunity to pursue early surveillance for malignancies, as well as genetic counseling.
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