• Title/Summary/Keyword: Pathology report

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Spontaneous Peripheral Ameloblastic Odontoma in a Male Sprague-Dawley Rat

  • Li, Yinghua;Bae, Han-Ik;Kim, Hak-Soo;Kang, Min-Soo;Gong, Bo-Ho;Jung, Won-Hee;Lee, Sranna;Bae, Jin-Sook;Kim, Kap-Ho;Song, Si-Whan;Lee, Jae-Hyun;Kang, Boo-Hyon
    • Toxicological Research
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    • v.33 no.2
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    • pp.141-147
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    • 2017
  • Peripheral ameloblastic odontoma is a rare variant of odontogenic tumor occurring in the extraosseous region. The present report describes a spontaneous tumor in male Sprague-Dawley (SD) rats. The clinically confirmed nodule in the right mandibular region was first observed when the rat was 42 weeks and remained until the terminal sacrifice date when the animal was 48 weeks of age. At necropsy, a well demarcated nodule, approximately $2.5{\times}2.0{\times}2.0cm$, protruded from the ventral area of the right mandible. The nodule was not attached to mandibular bone and was not continuous with the normal teeth. Histopathologically, the tumor was characterized by the simultaneous occurrence of an ameloblastomatous component and composite odontoma-like elements within the same tumor. The epithelial portion formed islands or cords resembling the follicle or plexiform pattern typical of ameloblastoma and was surrounded by mesenchymal tissue. Formation of eosinophilic and basophilic hard tissue matrix (dentin and enamel) resembling odontoma was observed in the center of the tumor. Mitotic figures were rare, and areas of cystic degeneration were present. Immunohistochemically, the epithelial component was positive for cytokeratin AE1/AE3 (CK AE1/AE3), and the mesenchymal component and odontoblast-like cells were positive for vimentin, in the same manner as in normal teeth. On the basis of these findings, the tumor was diagnosed as a peripheral ameloblastic odontoma in an extraosseous mandibular region in a SD rat. In the present study, we report the uncommon spontaneous peripheral ameloblastic odontoma in the SD rat. We also discuss here the morphological characteristics, origin, histochemical, and immunohistochemical features for the diagnosis of this tumor.

Fine Needle Aspiration Cytological Findings of Angioimmunoblastic T-cell Lymphoma -A Brief Case Report - (혈관면역모세포 T세포 림프종의 세침흡인 세포소견 -짧은 증례 보고-)

  • Jung, Ji-Han;Choi, Hyun-Joo;Kang, Seok-Jin;Kang, Chang-Suk;Lee, Kyo-Young;Yoo, Jin-Young
    • The Korean Journal of Cytopathology
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    • v.17 no.2
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    • pp.159-161
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    • 2006
  • Recently, we experienced a case of Angioimmunoblastic T-cell lymphom (AITL) in a 60-year-old man presented with lymphadenopathy, which is first cytological report in Korea. The cytological features showed a heterogeneous population of small to medium-sized lymphocytes, immunoblasts, and plasma cells. Characteristically, there were also a distinct population of follicular dendritic cells admixed with lymphoid cells, forming the so-called dendritic cell-lymphocyte complexes. Histological features showed the classic morphologic features of AITL. Recognition of the characteristic cytological features can suggest the possibility of AITL.

Fine Needle Aspiration Cytology of Pilomatrixoma - Two Cases Report - (모기질세포종의 세침흡인 세포학적 소견 - 2예 보고 -)

  • Paik, Seung-Sam;Kim, Dong-Hoon;Lee, How-Jin;Jang, Se-Jin;Park, Moon-Hyang;Lee, Jung-Dal
    • The Korean Journal of Cytopathology
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    • v.8 no.2
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    • pp.155-159
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    • 1997
  • Pilomatrixoma is a benign skin appendage tumor of hair matrix cell origin. The cytological appearance of this tumor may cause problems when attempting to establish a differential diagnosis with other neoplasms. Herein we report the aspiration cytology findings of two cases of pilomatrixoma. One case was diagnosed as atypical cell clusters initially and the other was diagnosed as pilomatrixoma. On cytologic examination, both cases showed clusters of tightly arranged basaloid cells with an uniform appearance, scanty cytoplasm and round hyperchromatic nuclei. There were histiocytes and multinucleated foreign body giant cells merged with the amorphous opaque orangeophilic materials of "ghost cells". The differential diagnosis with other neoplasms is discussed.

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