The American Journal of Surgical Pathology · 2008 · 107 citations · 27 references
MedicineOncologyPathologyDna RepairMolecular OncologyNeoplasiaCancer Genomic InstabilityCutaneous NeoplasmsDna Repair DefectsMalignant NeoplasmsMicrosatellite InstabilitySkin TumorsCancer-associated Defects In Nucleotide Excision RepairColonic PathologyDna Mismatch RecognitionDna Mismatch Repair DeficiencyGastrointestinal MalignancyHistologic ExaminationMismatch Repair Gene MutationsSebaceous Neoplasms
Cutaneous sebaceous neoplasia is known to exhibit a high degree of DNA mismatch repair (MMR) deficiency leading to microsatellite instability and these tumors can be markers of the Muir-Torre syndrome and internal malignancy. Other tumors, such as colonic carcinoma, show tendencies toward particular histologic features and sites of involvement correlating with MMR deficiency. There are few comprehensive studies of unselected cutaneous sebaceous neoplasms. To address this gap in knowledge, we examined 94 sebaceous neoplasms from 92 patients and 17 sebaceous hyperplasia controls using immunohistochemistry for MLH1, MSH2, and MSH6. Our results indicate that MMR deficiency is significantly associated with anatomic location (more frequently in the trunk and extremities as compared with head and neck), tumor type (more often in adenoma compared with carcinoma within the head and neck region), and architecture (keratoacanthomalike). No correlation between cystic change and MMR deficiency was noted. Cutaneous sebaceous neoplasia has tendencies toward certain tumor types and anatomic distribution based on MMR status analogous to that seen in colonic carcinomas and other tumors. These may be helpful indicators for further workup for the Muir-Torre syndrome.
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Douglas Torre · Archives of Dermatology · 1968 · 349 citations
Roland Kruse, Arno Rütten, Christof Lamberti et al. · The American Journal of Human Genetics · 1998 · 234 citations · Full text