| Literature DB >> 34912152 |
Kanika Sharma1, Minu Bajpai1, Rajni Yadav2, Prabudh Goel1.
Abstract
The rarity, diverse clinical presentation, relatively featureless sonography, and diagnostic dilemma associated with pilomatrixomas may trigger anxiety and call for unwarranted investigations. The authors have shared their experience in two consecutive cases to generate awareness for such lesions. Copyright:Entities:
Keywords: Basaloid cells; calcifying epithelioma of Malherbe; ghost cells; pilomatrixoma
Year: 2021 PMID: 34912152 PMCID: PMC8637976 DOI: 10.4103/jiaps.JIAPS_269_20
Source DB: PubMed Journal: J Indian Assoc Pediatr Surg ISSN: 0971-9261
Figure 1Pilomatrixoma. Clinical picture of the solitary lesion on medial aspect of left leg; with excised specimen (inset)
Figure 2The triad of ghost cells, basaloid cells with high nuclear: cytoplasmic ratio and chromatin/foreign body giant cells inside the nuclei are suggestive of Pilomatrixoma. Case 1 (a) The tumor shows nests of basaloid cells (black arrow) with abrupt trichilemmal type of keratinization and presence of ghost cells (blue arrow) ×200, H and E (left). Foci of calcification (black arrow) seen ×100, H and E (middle). Foreign body giant cell reaction (blue arrow) ×100, H and E (right). Case 2 (b) The tumor is composed of islands of basaloid cells which show abrupt trichilemmal type of keratinization and ghost cells in the center of the islands, ×100 (left and middle), ×200 (right) H and E