Peutz-Jeghers syndrome a review of gynecological implications and the management of these patients through the presentation of a case report

Background: Peutz-Jeghers Syndrome (PJS) is a rare autosomal dominant genetic condition caused by mutations in STK11 (Serine/threonine kinase 11) gene (OMIM 602216 Serine/Threonine Protein Kinase 11) located in the short arm of chromosome 19 (19p.13.3). Case: We report the case of a 4 and ½ year-old...

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主要な著者: Katarzyna Plagens-Rotman (著者), Grażyna Jarząbek-Bielecka (著者), Piotr Merks (著者), Katarzyna Wróblewska-Seniuk (著者), Małgorzata Mizgier (著者), Ewa Jakubek (著者), Samuel Grześkiewicz (著者), Małgorzata Wójcik (著者), Witold Kędzia (著者)
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出版事項: IMR Press, 2022-04-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Katarzyna Plagens-Rotman  |e author 
700 1 0 |a Grażyna Jarząbek-Bielecka  |e author 
700 1 0 |a Piotr Merks  |e author 
700 1 0 |a Katarzyna Wróblewska-Seniuk  |e author 
700 1 0 |a Małgorzata Mizgier  |e author 
700 1 0 |a Ewa Jakubek  |e author 
700 1 0 |a Samuel Grześkiewicz  |e author 
700 1 0 |a Małgorzata Wójcik  |e author 
700 1 0 |a Witold Kędzia  |e author 
245 0 0 |a Peutz-Jeghers syndrome a review of gynecological implications and the management of these patients through the presentation of a case report 
260 |b IMR Press,   |c 2022-04-01T00:00:00Z. 
500 |a 0390-6663 
500 |a 10.31083/j.ceog4904085 
520 |a Background: Peutz-Jeghers Syndrome (PJS) is a rare autosomal dominant genetic condition caused by mutations in STK11 (Serine/threonine kinase 11) gene (OMIM 602216 Serine/Threonine Protein Kinase 11) located in the short arm of chromosome 19 (19p.13.3). Case: We report the case of a 4 and ½ year-old female child with a rare Peutz-Jeghers Syndrome. She was admitted to the Clinic of Gynaecology, the Faculty of Perinatology and Gynaecology, Chair of Adolescence Gynaecology and Sexology at Poznan University of Medical Sciences, in order to undergo preventive medical examinations. The patient was accompanied by her mother. Age and sex-appropriate development. Age-appropriate dental condition. Gynaecological examination was conducted. No changes were identified through palpation. Normal ultrasound picture. No symptoms of genital mucosa estrogenization, which is typical of the patient's age. A small amount of vaginal discharge was found. Pap smear was conducted to assess vaginal biocenosis. Lacidobacilli deficiency was found and feminine hygiene products, such as Iladian, were recommended. Melanotic macules around the mouth, typical of Peutz-Jeghers Syndrome were identified. Conclusions: Due to the increased cancer risk in patients with Peutz-Jeghers Syndrome, more frequent medical and gynaecological examinations are recommended for the girl. It should be noted that the girl's mother decision to have her daughter examined at such a young age was appropriate. 
546 |a EN 
690 |a children 
690 |a polyposis 
690 |a peutz-jeghers syndrome 
690 |a Gynecology and obstetrics 
690 |a RG1-991 
655 7 |a article  |2 local 
786 0 |n Clinical and Experimental Obstetrics & Gynecology, Vol 49, Iss 4, p 85 (2022) 
787 0 |n https://www.imrpress.com/journal/CEOG/49/4/10.31083/j.ceog4904085 
787 0 |n https://doaj.org/toc/0390-6663 
856 4 1 |u https://doaj.org/article/4fc835ca736b4bb4ad3db3a0ec4d59ef  |z Connect to this object online.