Skip to main content
Erschienen in: Familial Cancer 4/2010

01.12.2010

Peutz-Jeghers syndrome: a study of long-term surgical morbidity and causes of mortality

verfasst von: Y. Nancy You, Bruce G. Wolff, Lisa A. Boardman, Douglas L. Riegert-Johnson, Rui Qin

Erschienen in: Familial Cancer | Ausgabe 4/2010

Einloggen, um Zugang zu erhalten

Abstract

Patients with Peutz-Jeghers syndrome (PJS) require lifelong multidisciplinary care for gastrointestinal polyposis and increased risk of cancer. Their long-term morbidities and causes of mortality are unknown. Patients with a definitive diagnosis of PJS (n = 54) were retrospectively reviewed for disease course and outcome. Operative details, pathology and complications were noted for those treated surgically (n = 33). Median follow-up was 7.0 years (interquartile range: 2–20). Two malignancies were found intra-operatively (duodenal and rectal adenocarcinoma). In the long-term, 42% underwent additional operations; 1 patient developed short bowel syndrome, while another, chronic partial bowel obstruction and pain. Twenty-one additional cancers were treated in 19 patients: gynecologic (11), lung (3), and prostate (2) being the most common. 16 patients (30%) were deceased, at a median age of 51 years. The cause of death was unknown in 4 patients, but was due exclusively to malignancies in all other patients, most commonly due to metastatic gynecologic cancer (5). The overall survival of PJS patients was significantly shorter than the expected survival of an age-and gender-matched reference population (P < 0.001). Given the morbidities associated with repeated operations and the risk for cancer-related mortality in the long-term, efforts should focus on minimizing the need for surgical intervention and optimizing cancer detection, treatment and prevention.
Literatur
1.
Zurück zum Zitat Giardiello FM, Welsh SB, Hamilton SR et al (1987) Increased risk of cancer in the Peutz-Jeghers syndrome. N Engl J Med 316:1511–1514CrossRefPubMed Giardiello FM, Welsh SB, Hamilton SR et al (1987) Increased risk of cancer in the Peutz-Jeghers syndrome. N Engl J Med 316:1511–1514CrossRefPubMed
2.
Zurück zum Zitat Boardman LA, Thibodeau SN, Schaid DJ et al (1998) Increased risk for cancer in patients with the Peutz-Jeghers syndrome. Ann Intern Med 128:896–899PubMed Boardman LA, Thibodeau SN, Schaid DJ et al (1998) Increased risk for cancer in patients with the Peutz-Jeghers syndrome. Ann Intern Med 128:896–899PubMed
3.
Zurück zum Zitat Giardiello FM, Brensinger JD, Tersmette AC et al (2000) Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterology 119:1447–1453CrossRefPubMed Giardiello FM, Brensinger JD, Tersmette AC et al (2000) Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterology 119:1447–1453CrossRefPubMed
4.
Zurück zum Zitat Spigelman AD, Arese P, Phillips RK (1995) Polyposis: the Peutz-Jeghers syndrome. Br J Surg 82:1311–1314CrossRefPubMed Spigelman AD, Arese P, Phillips RK (1995) Polyposis: the Peutz-Jeghers syndrome. Br J Surg 82:1311–1314CrossRefPubMed
5.
Zurück zum Zitat Hearle N, Schumacher V, Menko FH et al (2006) Frequency and spectrum of cancers in the Peutz-Jeghers syndrome. Clin Cancer Res 12:3209–3215CrossRefPubMed Hearle N, Schumacher V, Menko FH et al (2006) Frequency and spectrum of cancers in the Peutz-Jeghers syndrome. Clin Cancer Res 12:3209–3215CrossRefPubMed
6.
Zurück zum Zitat Giardiello FM, Trimbath JD (2006) Peutz-Jeghers syndrome and management recommendations. Clin Gastroenterol Hepatol 4:408–415CrossRefPubMed Giardiello FM, Trimbath JD (2006) Peutz-Jeghers syndrome and management recommendations. Clin Gastroenterol Hepatol 4:408–415CrossRefPubMed
7.
Zurück zum Zitat Hinds R, Philp C, Hyer W et al (2004) Complications of childhood Peutz-Jeghers syndrome: implications for pediatric screening. J Pediatr Gastroenterol Nutr 39:219–220CrossRefPubMed Hinds R, Philp C, Hyer W et al (2004) Complications of childhood Peutz-Jeghers syndrome: implications for pediatric screening. J Pediatr Gastroenterol Nutr 39:219–220CrossRefPubMed
8.
Zurück zum Zitat Lin BC, Lien JM, Chen RJ et al (2000) Combined endoscopic and surgical treatment for the polyposis of Peutz-Jeghers syndrome. Surg Endosc 14:1185–1187CrossRefPubMed Lin BC, Lien JM, Chen RJ et al (2000) Combined endoscopic and surgical treatment for the polyposis of Peutz-Jeghers syndrome. Surg Endosc 14:1185–1187CrossRefPubMed
9.
Zurück zum Zitat Spigelman AD, Thomson JP, Phillips RK (1990) Towards decreasing the relaparotomy rate in the Peutz-Jeghers syndrome: the role of peroperative small bowel endoscopy. Br J Surg 77:301–302CrossRefPubMed Spigelman AD, Thomson JP, Phillips RK (1990) Towards decreasing the relaparotomy rate in the Peutz-Jeghers syndrome: the role of peroperative small bowel endoscopy. Br J Surg 77:301–302CrossRefPubMed
10.
Zurück zum Zitat Oncel M, Remzi FH, Church JM et al (2004) Benefits of ‘clean sweep’ in Peutz-Jeghers patients. Colorectal Dis 6:332–335CrossRefPubMed Oncel M, Remzi FH, Church JM et al (2004) Benefits of ‘clean sweep’ in Peutz-Jeghers patients. Colorectal Dis 6:332–335CrossRefPubMed
11.
Zurück zum Zitat Edwards DP, Khosraviani K, Stafferton R et al (2003) Long-term results of polyp clearance by intraoperative enteroscopy in the Peutz-Jeghers syndrome. Dis Colon Rectum 46:48–50CrossRefPubMed Edwards DP, Khosraviani K, Stafferton R et al (2003) Long-term results of polyp clearance by intraoperative enteroscopy in the Peutz-Jeghers syndrome. Dis Colon Rectum 46:48–50CrossRefPubMed
12.
Zurück zum Zitat Spigelman AD, Murday V, Phillips RK (1989) Cancer and the Peutz-Jeghers syndrome. Gut 30:1588–1590CrossRefPubMed Spigelman AD, Murday V, Phillips RK (1989) Cancer and the Peutz-Jeghers syndrome. Gut 30:1588–1590CrossRefPubMed
13.
Zurück zum Zitat Schumacher V, Vogel T, Leube B et al (2005) STK11 genotyping and cancer risk in Peutz-Jeghers syndrome. J Med Genet 42:428–435CrossRefPubMed Schumacher V, Vogel T, Leube B et al (2005) STK11 genotyping and cancer risk in Peutz-Jeghers syndrome. J Med Genet 42:428–435CrossRefPubMed
15.
Zurück zum Zitat Jansen M, Ten Klooster JP, Offerhaus GJ et al (2009) LKB1 and AMPK family signaling: the intimate link between cell polarity and energy metabolism. Physiol Rev 89:777–798CrossRefPubMed Jansen M, Ten Klooster JP, Offerhaus GJ et al (2009) LKB1 and AMPK family signaling: the intimate link between cell polarity and energy metabolism. Physiol Rev 89:777–798CrossRefPubMed
16.
Zurück zum Zitat Dunlop MG.(2002) Guidance on gastrointestinal surveillance for hereditary non-polyposis colorectal cancer, familial adenomatous polypolis, juvenile polyposis, and Peutz-Jeghers syndrome. Gut. 51 Suppl 5: V21-7 Dunlop MG.(2002) Guidance on gastrointestinal surveillance for hereditary non-polyposis colorectal cancer, familial adenomatous polypolis, juvenile polyposis, and Peutz-Jeghers syndrome. Gut. 51 Suppl 5: V21-7
17.
Zurück zum Zitat McGrath DR, Spigelman AD (2001) Preventive measures in Peutz-Jeghers syndrome. Fam Cancer 1:121–125CrossRefPubMed McGrath DR, Spigelman AD (2001) Preventive measures in Peutz-Jeghers syndrome. Fam Cancer 1:121–125CrossRefPubMed
18.
Zurück zum Zitat Linos DA, Dozois RR, Dahlin DC et al (1981) Does Peutz-Jeghers syndrome predispose to gastrointestinal malignancy? a later look. Arch Surg 116:1182–1184PubMed Linos DA, Dozois RR, Dahlin DC et al (1981) Does Peutz-Jeghers syndrome predispose to gastrointestinal malignancy? a later look. Arch Surg 116:1182–1184PubMed
19.
Zurück zum Zitat Shepherd NA, Bussey HJ, Jass JR (1987) Epithelial misplacement in Peutz-Jeghers polyps. A diagnostic pitfall. Am J Surg Pathol 11:743–749CrossRefPubMed Shepherd NA, Bussey HJ, Jass JR (1987) Epithelial misplacement in Peutz-Jeghers polyps. A diagnostic pitfall. Am J Surg Pathol 11:743–749CrossRefPubMed
20.
Zurück zum Zitat Bergstralh E, Offord K (1988) Conditional probabilities used in calculating cohort expected survival. Section of Biostatics, Mayo Clin Tech Report Bergstralh E, Offord K (1988) Conditional probabilities used in calculating cohort expected survival. Section of Biostatics, Mayo Clin Tech Report
21.
Zurück zum Zitat Dozois RR, Judd ES, Dahlin DC et al (1969) The Peutz-Jeghers syndrome. Is there a predisposition to the development of intestinal malignancy? Arch Surg 98:509–517PubMed Dozois RR, Judd ES, Dahlin DC et al (1969) The Peutz-Jeghers syndrome. Is there a predisposition to the development of intestinal malignancy? Arch Surg 98:509–517PubMed
22.
Zurück zum Zitat Riegert-Johnson DL, Boardman LA. Peutz-Jeghers syndrome. In Riegert-Johnson DL, Boardman LA (eds): Familial Cancer Syndromes. ed. Bethesda: National Institute of Health 2009 (In press) Riegert-Johnson DL, Boardman LA. Peutz-Jeghers syndrome. In Riegert-Johnson DL, Boardman LA (eds): Familial Cancer Syndromes. ed. Bethesda: National Institute of Health 2009 (In press)
23.
Zurück zum Zitat Rebsdorf Pedersen I, Hartvigsen A, Fischer Hansen B et al (1994) Management of Peutz-Jeghers syndrome Experience with patients from the Danish Polyposis Register. Int J Colorectal Dis 9:177–179CrossRefPubMed Rebsdorf Pedersen I, Hartvigsen A, Fischer Hansen B et al (1994) Management of Peutz-Jeghers syndrome Experience with patients from the Danish Polyposis Register. Int J Colorectal Dis 9:177–179CrossRefPubMed
24.
Zurück zum Zitat Amaro R, Diaz G, Schneider J et al (2000) Peutz-Jeghers syndrome managed with a complete intraoperative endoscopy and extensive polypectomy. Gastrointest Endosc 52:552–554CrossRefPubMed Amaro R, Diaz G, Schneider J et al (2000) Peutz-Jeghers syndrome managed with a complete intraoperative endoscopy and extensive polypectomy. Gastrointest Endosc 52:552–554CrossRefPubMed
25.
Zurück zum Zitat Panos RG, Opelka FG, Nogueras JJ (1990) Peutz-Jeghers syndrome. A call for intraoperative enteroscopy. Am Surg 56:331–333PubMed Panos RG, Opelka FG, Nogueras JJ (1990) Peutz-Jeghers syndrome. A call for intraoperative enteroscopy. Am Surg 56:331–333PubMed
26.
Zurück zum Zitat Seenath MM, Scott MJ, Morris AI et al (2003) Combined surgical and endoscopic clearance of small-bowel polyps in Peutz-Jeghers syndrome. J R Soc Med 96:505–506CrossRefPubMed Seenath MM, Scott MJ, Morris AI et al (2003) Combined surgical and endoscopic clearance of small-bowel polyps in Peutz-Jeghers syndrome. J R Soc Med 96:505–506CrossRefPubMed
27.
Zurück zum Zitat Cunningham JD, Vine AJ, Karch L et al (1998) The role of laparoscopy in the management of intussusception in the Peutz-Jeghers syndrome: case report and review of the literature. Surg Laparosc Endosc 8:17–20CrossRefPubMed Cunningham JD, Vine AJ, Karch L et al (1998) The role of laparoscopy in the management of intussusception in the Peutz-Jeghers syndrome: case report and review of the literature. Surg Laparosc Endosc 8:17–20CrossRefPubMed
28.
Zurück zum Zitat Zanoni EC, Averbach M, Borges JL et al (2003) Laparoscopic treatment of intestinal intussusception in the Peutz-Jeghers syndrome: case report and review of the literature. Surg Laparosc Endosc Percutan Tech 13:280–282CrossRefPubMed Zanoni EC, Averbach M, Borges JL et al (2003) Laparoscopic treatment of intestinal intussusception in the Peutz-Jeghers syndrome: case report and review of the literature. Surg Laparosc Endosc Percutan Tech 13:280–282CrossRefPubMed
29.
Zurück zum Zitat Pelizzo G, Martelossi S, Popoiu MC et al (2007) Laparoendoscopically assisted endoscopic small bowel polypectomy in a patient with Peutz-Jeghers syndrome. J Laparoendosc Adv Surg Tech A 17:140–142CrossRefPubMed Pelizzo G, Martelossi S, Popoiu MC et al (2007) Laparoendoscopically assisted endoscopic small bowel polypectomy in a patient with Peutz-Jeghers syndrome. J Laparoendosc Adv Surg Tech A 17:140–142CrossRefPubMed
30.
Zurück zum Zitat The National Comprehensive Cancer Network Oncology Practice Guidelines on Colorectal Cancer Screening. www.nccn.org. V.1. 2010. Date accessed: May 1, 2010 The National Comprehensive Cancer Network Oncology Practice Guidelines on Colorectal Cancer Screening. www.​nccn.​org. V.1. 2010. Date accessed: May 1, 2010
31.
Zurück zum Zitat De Leng WW, Westerman AM, Weterman MA et al (2003) Cyclooxygenase 2 expression and molecular alterations in Peutz-Jeghers hamartomas and carcinomas. Clin Cancer Res 9:3065–3072PubMed De Leng WW, Westerman AM, Weterman MA et al (2003) Cyclooxygenase 2 expression and molecular alterations in Peutz-Jeghers hamartomas and carcinomas. Clin Cancer Res 9:3065–3072PubMed
32.
Zurück zum Zitat Wei C, Amos CI, Zhang N et al (2008) Suppression of Peutz-Jeghers polyposis by targeting mammalian target of rapamycin signaling. Clin Cancer Res 14:1167–1171CrossRefPubMed Wei C, Amos CI, Zhang N et al (2008) Suppression of Peutz-Jeghers polyposis by targeting mammalian target of rapamycin signaling. Clin Cancer Res 14:1167–1171CrossRefPubMed
33.
Zurück zum Zitat Perzin KH, Bridge MF (1982) Adenomatous and carcinomatous changes in hamartomatous polyps of the small intestine (Peutz-Jeghers syndrome): report of a case and review of the literature. Cancer 49:971–983CrossRefPubMed Perzin KH, Bridge MF (1982) Adenomatous and carcinomatous changes in hamartomatous polyps of the small intestine (Peutz-Jeghers syndrome): report of a case and review of the literature. Cancer 49:971–983CrossRefPubMed
34.
Zurück zum Zitat Miller LJ, Bartholomew LG, Dozois RR et al (1983) Adenocarcinoma of the rectum arising in a hamartomatous polyp in a patient with Peutz-Jeghers syndrome. Dig Dis Sci 28:1047–1051CrossRefPubMed Miller LJ, Bartholomew LG, Dozois RR et al (1983) Adenocarcinoma of the rectum arising in a hamartomatous polyp in a patient with Peutz-Jeghers syndrome. Dig Dis Sci 28:1047–1051CrossRefPubMed
35.
Zurück zum Zitat Flageole H, Raptis S, Trudel JL et al (1994) Progression toward malignancy of hamartomas in a patient with Peutz-Jeghers syndrome: case report and literature review. Can J Surg 37:231–236PubMed Flageole H, Raptis S, Trudel JL et al (1994) Progression toward malignancy of hamartomas in a patient with Peutz-Jeghers syndrome: case report and literature review. Can J Surg 37:231–236PubMed
36.
Zurück zum Zitat de Leng WW, Jansen M, Keller JJ et al (2007) Peutz-Jeghers syndrome polyps are polyclonal with expanded progenitor cell compartment. Gut 56:1475–1476CrossRefPubMed de Leng WW, Jansen M, Keller JJ et al (2007) Peutz-Jeghers syndrome polyps are polyclonal with expanded progenitor cell compartment. Gut 56:1475–1476CrossRefPubMed
Metadaten
Titel
Peutz-Jeghers syndrome: a study of long-term surgical morbidity and causes of mortality
verfasst von
Y. Nancy You
Bruce G. Wolff
Lisa A. Boardman
Douglas L. Riegert-Johnson
Rui Qin
Publikationsdatum
01.12.2010
Verlag
Springer Netherlands
Erschienen in
Familial Cancer / Ausgabe 4/2010
Print ISSN: 1389-9600
Elektronische ISSN: 1573-7292
DOI
https://doi.org/10.1007/s10689-010-9358-1

Weitere Artikel der Ausgabe 4/2010

Familial Cancer 4/2010 Zur Ausgabe

Adjuvante Immuntherapie verlängert Leben bei RCC

25.04.2024 Nierenkarzinom Nachrichten

Nun gibt es auch Resultate zum Gesamtüberleben: Eine adjuvante Pembrolizumab-Therapie konnte in einer Phase-3-Studie das Leben von Menschen mit Nierenzellkarzinom deutlich verlängern. Die Sterberate war im Vergleich zu Placebo um 38% geringer.

Alectinib verbessert krankheitsfreies Überleben bei ALK-positivem NSCLC

25.04.2024 NSCLC Nachrichten

Das Risiko für Rezidiv oder Tod von Patienten und Patientinnen mit reseziertem ALK-positivem NSCLC ist unter einer adjuvanten Therapie mit dem Tyrosinkinase-Inhibitor Alectinib signifikant geringer als unter platinbasierter Chemotherapie.

Bei Senioren mit Prostatakarzinom auf Anämie achten!

24.04.2024 DGIM 2024 Nachrichten

Patienten, die zur Behandlung ihres Prostatakarzinoms eine Androgendeprivationstherapie erhalten, entwickeln nicht selten eine Anämie. Wer ältere Patienten internistisch mitbetreut, sollte auf diese Nebenwirkung achten.

ICI-Therapie in der Schwangerschaft wird gut toleriert

Müssen sich Schwangere einer Krebstherapie unterziehen, rufen Immuncheckpointinhibitoren offenbar nicht mehr unerwünschte Wirkungen hervor als andere Mittel gegen Krebs.

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.