Predisposition of papillary thyroid carcinoma in a family dignosed as hereditary breast and ovarian cancer syndrome

Herediter meme over kanser sendromu, erken dönemde tanı alan ailesel tip meme ve/veya overkanseri ile karakterizedir. Ailelerde prostat ve pankreas kanserine yatkınlık görülebilir. Yazımızdaherediter meme-over kanser sendromu tanısı almış bir aile sunulmakta vebu ailede sık gözlenenpapiller tip tiroid kanserini oluşturabilecek nedenler tartışılmaktadır. Ailede BRCA 1 ve BRCA 2genlerinin belli bölgelerinde mutasyon gösterilmemiştir. Ancak klinik olarak meme over kansersendromu tanısı alan aile literatüre göre papiller tiroid kanserine yatkınlıkla tanımlanan tekörnektir. Burada tanımlanan farklı tümör tiplerinde etkilenen ortak bir mekanizma olduğudüşünülebilir. Sonuç olarak, papiller tiroid kansere yatkınlığı olan herediter meme-over kansersendromu tanısı almış nadir ailelerde etkilenen yolakları bulmak için daha fazla araştırmaya gerekvardır.

Herediter meme over kanser sendrom tanısı almış ailede tiroid papiller kanser birlikteliği

Hereditary breast and ovarian cancer syndrome is characterized by the familial type of breastand/or ovarian cancers diagnosed at early onset. In these families, predisposition to prostate andpancreas cancers can be seen. Here a family who had hereditary breast and ovarian cancersyndrome was presented and we also discussed the possible mechanisms in the predisposition ofpapillar type thyroid cancer which is common in this family. No BRCA 1 and BRCA 2 mutationhad been observed in certain loci in this family. Due to the literature findings, our family is thesole example which has clinically hereditary breast and ovarian cancer syndrome diagnosis withthyroid papillary carcinoma predisposition.Here, there may be a common mechanism affected inthese different tumors. So, further studies are necessary to find out affected pathways in patientshaving hereditary type breast and ovarian cancer who has also predispositionto papillary thyroidcarcinoma.

___

  • 1. Shulman LP. Hereditary breast and ovarian cancer (HBOC): clinical features and counseling for BRCA1 and BRCA2, Lynch syndrome, Cowden syndrome, and Li-Fraumeni syndrome. Obstet Gynecol Clin North Am 2010; 37: 109-33.
  • 2. Martin SA, Hewish M, Lord CJ, Ashworth A. Genomic instability and the selection of treatments for cancer. J Pathol 2010; 220: 281-9.
  • 3. Hemminki K, Eng C, Chen B. Familial risks for nonmedullary thyroid cancer. J Clin Endocrinol Metab 2005; 90: 5747-53.
  • 4. Güran S, Safali M. A case of neurofibromatosis and breast cancer: loss of heterozygosity of NF1 in breast cancer. Cancer Genet Cytogenet 2005; 156: 86-8.
  • 5. Güran S, Ozet A, Dede M, Gille JJ, Yenen MC. Hereditary breast cancer syndromes in a Turkish population. Results of molecular germline analysis. Cancer Genet Cytogenet 2005; 160: 164-8.
  • 6. Saxena R, Kohli S, Guleria K, Verma IC. Novel human pathological mutations. Gene symbol: TP53. Disease: Li-Fraumeni syndrome. Hum Genet 2010; 127: 480.
  • 7. Lynch HT, Casey MJ, Snyder CL, Bewtra C, Lynch JF, Butts M, Godwin AK. Hereditary ovarian carcinoma: heterogeneity, molecular genetics, pathology, and management. Mol Oncol 2009; 3: 97-137.
  • 8. Goldberg JI, Borgen PI. Breast cancer susceptibility testing: past, present and future. Expert Rev Anticancer Ther 2006; 6: 1205-14.
  • 9. Bahçe M. Genetics in ovarian tumors. Turkiye Klinikleri J Surg Med Sci 2007; 3: 5-9.
  • 10. Hitchins MP, Ward RL. Constitutional (germline) MLH1 epimutation as an aetiological mechanism for hereditary non-polyposis colorectal cancer. J Med Genet 2009; 46: 793-802.
  • 11. Landi S. Genetic predisposition and environmental risk factors to pancreatic cancer: A review of the literature. Mutat Res 2009; 681: 299-307.
  • 12. Futreal PA, Coin L, Marshall M, Down T, Hubbard T, Wooster R, Rahman N, Stratton MR. A census of human cancer genes. Nat Rev Cancer 2004; 4: 177-83.
  • 13. Jensen UB, Sunde L, Timshel S, Halvarsson B, Nissen A, Bernstein I, Nilbert M. Mismatch repair defective breast cancer in the hereditary nonpolyposis colorectal cancer syndrome. Breast Cancer Res Treat 2010; 120: 777-82.
  • 14. Yağcı G, Dede M, Guran S, Yenen MC, Durukan AH, Safali M. A papillary thyroid carcinoma case associated with hereditary colon carcinoma due to familial adenomatous polyposis with no hereditary mutation finding. Int J Colorectal Dis 2007; 22: 725-6.
  • 15. Nagy R, Sweet K, Eng C. Highly penetrant hereditary cancer syndromes. Oncogene 2004; 23: 6445-70.
  • 16. Oğur G: Genes, chromosomes and cancer. Turkiye Klinikleri J Pediatr Sci 2005; 1: 73-92.
Cumhuriyet Tıp Dergisi (ELEKTRONİK)-Cover
  • Yayın Aralığı: Yılda 4 Sayı
  • Yayıncı: Cumhuriyet Üniversitesi Tıp Fakültesi
Sayıdaki Diğer Makaleler

Early period results of arthroscopic anterior cruciate ligament reconstruction with quadrupled hamstring autograft

Ali ÖÇGÜDER, Barış KILINÇ, Ahmet FIRAT, Selim ŞANEL, Metin ÖZDEMİR, Ali Kağan GÖKAKIN

Epitel hücre anormalliği saptanan servikal smear olgularında sitolojik tanı dağılımı ve sito- histopatolojik korelasyon

Hande KESER, Şahande ELAGÖZ, Ersin TUNCER, Hatice ÖZER, Handan AKER, Abdullah BOZTOSUN, Ayşe ÇİFTÇİ

Apendiks mukoseli radyolojik tanısı

Ahmet MÜSLEHİDDİNOĞLU, İsmail ŞALK, Kayhan KARAKUŞ, Hacı Ahmet SÜMBÜL

Conversion to open surgery in the era of laparoscopic cholecystectomy: Rates and reasons

Mustafa ATABEY, Cengiz AYDIN, Boran Cihat KARAKUŞ, Ali Kağan GÖKAKIN

Pierre Robin sendromlu olguda anestezi sırasında görülen ani kardiak arrest

Ahmet Cemil İSBİR, Caner MİMAROĞLU, Cevdet DÜGER, İclal KOL ÖZDEMİR, Sinan GÜRSOY, Kenan KAYGUSUZ

İdiyopatik myelofibrozis tanılı olguda adaptif splenik radyoterapi

Mehmet Fuat EREN, Ayfer AY

Beyin tümörlü hastaların radyoterapi sonrası retrospektif değerlendirilmesi

Turgut KAÇAN, Ebru AKKAŞ ATASEVER, Eda ERDİŞ, Yıllar OKUR, Mehmet Fuat EREN, Birsen YÜCEL, Nalan BABACAN, Saadettin KILIÇKAP

Monilethrix

Derya YÜKSEL, Yunus SARAL, Ahmet METİN, Nursel DİLEK

Kronik Obstrüktif Akciğer Hastalığı olan bireylerin yeti yitimi, anksiyete ve depresyon yönünden değerlendirilmesi

Bilgen Begüm AFŞAR, Esen AKKAYA, Sevinç BİLGİN, Murat YALÇINSOY, Halil İbrahim YAKAR

Does the symmetry of the breasts continue after breast augmentation?

Nazım GÜMÜŞ, Sarper YILMAZ