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About 1,251 results

ALLMedicine™ Peutz-Jeghers Syndrome Center

Research & Reviews  617 results

Intestinal obstruction with oral pigmentation: a clue to Peutz-Jeghers syndrome.
https://doi.org/10.1136/bcr-2020-239079
BMJ Case Reports; Sahoo A, Singh P et. al.

Apr 2nd, 2021 - Peutz-Jeghers syndrome (PJS) is an autosomal dominant disorder, which manifests as mucocutaneous hyperpigmentation and, intestinal and extraintestinal polyps. The classic triad of abdominal pain, mass and jam-like stools are not found commonly. On...

Non-Peutz-Jeghers syndrome-associated ovarian sex cord tumor with annular tubules treat...
https://doi.org/10.1177/0300060521996563
The Journal of International Medical Research; Li C, Aishajiang R et. al.

Mar 15th, 2021 - There are no standard treatment options for metastatic and recurrent non-Peutz-Jeghers syndrome (PJS)-associated sex cord tumor with annular tubules (SCTAT). The effects of chemotherapy and/or radiotherapy are still not well-defined. Herein, we pr...

Ileoileal intussusception treated by polypectomy with spiral enteroscopy in Peutz-Jeghe...
https://doi.org/10.1055/a-1382-8060
Endoscopy Lafeuille P, Calavas L et. al.

Mar 8th, 2021 - Ileoileal intussusception treated by polypectomy with spiral enteroscopy in Peutz-Jeghers syndrome.|2021|Lafeuille P,Calavas L,Ragi O,Lambin T,Pioche M,|

Peutz-Jeghers syndrome.
https://doi.org/10.1097/MOG.0000000000000718 10.1007/s10689-020-00191-4. 10.1055/a-1276-6452.
Current Opinion in Gastroenterology; Tacheci I, Kopacova M et. al.

Feb 16th, 2021 - Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined by gastrointestinal hamartomas and mucocutaneous pigmentations, caused by a germline mutation in the serine/ threonine kinase 11 or liver kinase B1 (STK11/...

Underwater Ischemic Polypectomy for Multiple Small Bowel Polyps in a Patient With Peutz...
https://doi.org/10.14309/ajg.0000000000001162
The American Journal of Gastroenterology; Suwa T, Imai K et. al.

Feb 9th, 2021 - Underwater Ischemic Polypectomy for Multiple Small Bowel Polyps in a Patient With Peutz-Jeghers Syndrome.|2021|Suwa T,Imai K,Hotta K,Ito S,Kishida Y,|methods,surgery,surgery,

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Guidelines  1 results

Hereditary Cancer Syndromes and Risk Assessment: ACOG COMMITTEE OPINION, Number 793.
https://doi.org/10.1097/AOG.0000000000003562
Obstetrics and Gynecology;

Nov 25th, 2019 - A hereditary cancer syndrome is a genetic predisposition to certain types of cancer, often with onset at an early age, caused by inherited pathogenic variants in one or more genes. Most hereditary cancer syndromes exhibit autosomal dominant inheri...

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Clinicaltrials.gov  627 results

Intestinal obstruction with oral pigmentation: a clue to Peutz-Jeghers syndrome.
https://doi.org/10.1136/bcr-2020-239079
BMJ Case Reports; Sahoo A, Singh P et. al.

Apr 2nd, 2021 - Peutz-Jeghers syndrome (PJS) is an autosomal dominant disorder, which manifests as mucocutaneous hyperpigmentation and, intestinal and extraintestinal polyps. The classic triad of abdominal pain, mass and jam-like stools are not found commonly. On...

Non-Peutz-Jeghers syndrome-associated ovarian sex cord tumor with annular tubules treat...
https://doi.org/10.1177/0300060521996563
The Journal of International Medical Research; Li C, Aishajiang R et. al.

Mar 15th, 2021 - There are no standard treatment options for metastatic and recurrent non-Peutz-Jeghers syndrome (PJS)-associated sex cord tumor with annular tubules (SCTAT). The effects of chemotherapy and/or radiotherapy are still not well-defined. Herein, we pr...

Ileoileal intussusception treated by polypectomy with spiral enteroscopy in Peutz-Jeghe...
https://doi.org/10.1055/a-1382-8060
Endoscopy Lafeuille P, Calavas L et. al.

Mar 8th, 2021 - Ileoileal intussusception treated by polypectomy with spiral enteroscopy in Peutz-Jeghers syndrome.|2021|Lafeuille P,Calavas L,Ragi O,Lambin T,Pioche M,|

Peutz-Jeghers syndrome.
https://doi.org/10.1097/MOG.0000000000000718 10.1007/s10689-020-00191-4. 10.1055/a-1276-6452.
Current Opinion in Gastroenterology; Tacheci I, Kopacova M et. al.

Feb 16th, 2021 - Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined by gastrointestinal hamartomas and mucocutaneous pigmentations, caused by a germline mutation in the serine/ threonine kinase 11 or liver kinase B1 (STK11/...

Underwater Ischemic Polypectomy for Multiple Small Bowel Polyps in a Patient With Peutz...
https://doi.org/10.14309/ajg.0000000000001162
The American Journal of Gastroenterology; Suwa T, Imai K et. al.

Feb 9th, 2021 - Underwater Ischemic Polypectomy for Multiple Small Bowel Polyps in a Patient With Peutz-Jeghers Syndrome.|2021|Suwa T,Imai K,Hotta K,Ito S,Kishida Y,|methods,surgery,surgery,

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News  2 results

Laugier-Hunziker Syndrome
https://www.mdedge.com/dermatology/article/148388/pigmentation-disorders/laugier-hunziker-syndrome/page/0/1

Sep 29th, 2017 - Benign hyperpigmentation of the lips and fingers has been reported. 1 The average age of onset of LHS is 52 years, and it typically is diagnosed in white adults.

Basal Cell Nevus Syndrome in a 9-Year-Old Boy
https://www.medscape.com/viewarticle/752297_2

Nov 1st, 2011 - What is the diagnosis? Your Peers Chose: Rombo syndrome 0% Gorlin syndrome 0% Brooke-Spiegler syndrome 0% Peutz-Jeghers syndrome 0% Cowden syndrome 0% A screening workup included an MRI of the brain and radiographs of the headand chest, all of whi...

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Patient Education  4 results see all →