LANGERHANS CELL SARCOMA INVOLVING THE ORAL CAVITY
Langerhans cell sarcoma (LCS) is a high-grade neoplasm with overtly malignant cytological features and a Langerhans cell phenotype. Only one previous case has been reported in the oral cavity. A 79-year-old male patient presented for evaluation of multiple lesions affecting the lower lip, hard palat...
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Published in: | Oral surgery, oral medicine, oral pathology and oral radiology Vol. 134; no. 3; p. e150 |
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Elsevier Inc
01-09-2022
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Abstract | Langerhans cell sarcoma (LCS) is a high-grade neoplasm with overtly malignant cytological features and a Langerhans cell phenotype. Only one previous case has been reported in the oral cavity. A 79-year-old male patient presented for evaluation of multiple lesions affecting the lower lip, hard palate, upper alveolar mucosa, and skin. Biopsy of the lesions affecting the lower lip and palate showed a proliferation of histiocytic cells presenting atypia, pleomorphism, and atypical mitoses. Diagnosis of LCS was supported by immunoreactivity of the neoplastic cells for S-100, CD1a, CD207, and CD83. The patient died from widespread disease 3 months after diagnosis. Due to its rarity, LCS poses a diagnostic problem in the oral cavity and should be considered in the differential diagnosis of histiocytic proliferations. |
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AbstractList | Langerhans cell sarcoma (LCS) is a high-grade neoplasm with overtly malignant cytological features and a Langerhans cell phenotype. Only one previous case has been reported in the oral cavity. A 79-year-old male patient presented for evaluation of multiple lesions affecting the lower lip, hard palate, upper alveolar mucosa, and skin. Biopsy of the lesions affecting the lower lip and palate showed a proliferation of histiocytic cells presenting atypia, pleomorphism, and atypical mitoses. Diagnosis of LCS was supported by immunoreactivity of the neoplastic cells for S-100, CD1a, CD207, and CD83. The patient died from widespread disease 3 months after diagnosis. Due to its rarity, LCS poses a diagnostic problem in the oral cavity and should be considered in the differential diagnosis of histiocytic proliferations. |
Author | Costa, Luiz Roberto Fernandes De Noronha Santos Netto, Juliana Miranda, Águida Maria Menezes Aguiar De Almeida, Oslei Paes Pires, Fábio Ramoa De Lima Morais, Thayná Melo López, Bruna Sena |
Author_xml | – sequence: 1 givenname: Thayná Melo surname: De Lima Morais fullname: De Lima Morais, Thayná Melo – sequence: 2 givenname: Águida Maria Menezes Aguiar surname: Miranda fullname: Miranda, Águida Maria Menezes Aguiar – sequence: 3 givenname: Juliana surname: De Noronha Santos Netto fullname: De Noronha Santos Netto, Juliana – sequence: 4 givenname: Bruna Sena surname: López fullname: López, Bruna Sena – sequence: 5 givenname: Luiz Roberto Fernandes surname: Costa fullname: Costa, Luiz Roberto Fernandes – sequence: 6 givenname: Oslei Paes surname: De Almeida fullname: De Almeida, Oslei Paes – sequence: 7 givenname: Fábio Ramoa surname: Pires fullname: Pires, Fábio Ramoa |
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