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Rare occurrence of coexistent squamous cell carcinoma and basal cell carcinoma in a case of Xeroderma Pigmentosum

Yıl 2020, Cilt: 5 Sayı: 2, 90 - 92, 31.08.2020
https://doi.org/10.25000/acem.720032

Öz

Xeroderma Pigmentosum is an inherited disorder of DNA repair characterised by defective nucleotide excision repair, which is involved in repairing ultraviolet rays induced cross linking of pyramidine residues. Affected individuals are at increased risk of development of mucocutaneous cancers at a much earlier age than normal. This genodermatosis affects both sexes and all races. The incidence in India is still unknown. We report one such case of a nine year old boy with co-existent squamous cell carcinoma and basal cell carcinoma of the face.

Kaynakça

  • 1.Weedon D.Weedon’s skin pathology.3rd ed. Churchill Livingstone Elsevier.Philadelphia.2010:p.274-76.
  • 2.Black JO. Xeroderma Pigmentosum. Head Neck Pathol. 2016;10(2):139–144. doi:10.1007/s12105-016-0707-8.
  • 3. Irvine AD, Mellerio JE. In: Burns T, Breathnach S, Cox N,Griffiths C (editors).Rook’s Textbook of Dermatology. 8th ed.Wiley Blackwell.West Sussex,UK.2010:p.15.70-15.74.
  • 4.Tamhankar PM, Iyer SV, Ravindran S, Gupta N, Kabra M, Nayak C, et al. Clinical profile and mutation analysis of xeroderma pigmentosum in Indian patients. Indian J Dermatol Venereol Leprol 2015;81:16-22.
  • 5. Kumar V, Abbas AK, Aster JC. Robbins and Cotran Pathologic Basis of Disease.9th ed.Elsevier Saunders. Philadelphia.2015:p.314-15.
  • 6.DiGiovanna JJ, Kraemer KH. Shining a light on xeroderma pigmentosum. J Invest Dermatol. 2012;132:785–96.
  • 7. Prabhu VV, Kale S, More S. Xeroderma pigmentosum: Composite cutaneous malignancies A nightmare. Indian J Paediatr Dermatol 2015;16:142-5.
  • 8.Halkud R, Shenoy AM, Naik SM, Chavan P, Sidappa KT, Biswas S. Xeroderma pigmentosum: clinicopathological review of the multiple oculocutaneous malignancies and complications. Indian J Surg Oncol. 2014;5(2):120–124.
  • 9.Chaudhary M, Jajoo SN, Agarwal R (2012) Xeroderma Pigmentosum: A Case Report of Two Siblings. J Immunodefic Disor 1:2.
Yıl 2020, Cilt: 5 Sayı: 2, 90 - 92, 31.08.2020
https://doi.org/10.25000/acem.720032

Öz

Kaynakça

  • 1.Weedon D.Weedon’s skin pathology.3rd ed. Churchill Livingstone Elsevier.Philadelphia.2010:p.274-76.
  • 2.Black JO. Xeroderma Pigmentosum. Head Neck Pathol. 2016;10(2):139–144. doi:10.1007/s12105-016-0707-8.
  • 3. Irvine AD, Mellerio JE. In: Burns T, Breathnach S, Cox N,Griffiths C (editors).Rook’s Textbook of Dermatology. 8th ed.Wiley Blackwell.West Sussex,UK.2010:p.15.70-15.74.
  • 4.Tamhankar PM, Iyer SV, Ravindran S, Gupta N, Kabra M, Nayak C, et al. Clinical profile and mutation analysis of xeroderma pigmentosum in Indian patients. Indian J Dermatol Venereol Leprol 2015;81:16-22.
  • 5. Kumar V, Abbas AK, Aster JC. Robbins and Cotran Pathologic Basis of Disease.9th ed.Elsevier Saunders. Philadelphia.2015:p.314-15.
  • 6.DiGiovanna JJ, Kraemer KH. Shining a light on xeroderma pigmentosum. J Invest Dermatol. 2012;132:785–96.
  • 7. Prabhu VV, Kale S, More S. Xeroderma pigmentosum: Composite cutaneous malignancies A nightmare. Indian J Paediatr Dermatol 2015;16:142-5.
  • 8.Halkud R, Shenoy AM, Naik SM, Chavan P, Sidappa KT, Biswas S. Xeroderma pigmentosum: clinicopathological review of the multiple oculocutaneous malignancies and complications. Indian J Surg Oncol. 2014;5(2):120–124.
  • 9.Chaudhary M, Jajoo SN, Agarwal R (2012) Xeroderma Pigmentosum: A Case Report of Two Siblings. J Immunodefic Disor 1:2.
Toplam 9 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Cerrahi
Bölüm Olgu Sunumu
Yazarlar

Suguna Venugopal Bu kişi benim 0000-0002-4809-3045

Aparna Muralidhar 0000-0002-4896-5800

Hemalata Mahantappa Bu kişi benim

Sadaf Ahmad Bu kişi benim 0000-0002-2847-3788

Yayımlanma Tarihi 31 Ağustos 2020
Yayımlandığı Sayı Yıl 2020 Cilt: 5 Sayı: 2

Kaynak Göster

Vancouver Venugopal S, Muralidhar A, Mahantappa H, Ahmad S. Rare occurrence of coexistent squamous cell carcinoma and basal cell carcinoma in a case of Xeroderma Pigmentosum. Arch Clin Exp Med. 2020;5(2):90-2.