A Rare Case of Lipidized Fibrous Histiocytoma of the Oral Cavity
Benign fibrous histiocytoma (FH) is a common cutaneous tumor that rarely occurs in the oral cavity. Lipidized FH is an uncommon variant characterized by abundant foam cells in collagenized stroma. To our knowledge, only a single case of oral lipidized FH affecting the tongue has been reported. We ex...
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Published in | Curēus (Palo Alto, CA) Vol. 17; no. 4; p. e82265 |
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Springer Nature B.V
14.04.2025
Cureus |
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Abstract | Benign fibrous histiocytoma (FH) is a common cutaneous tumor that rarely occurs in the oral cavity. Lipidized FH is an uncommon variant characterized by abundant foam cells in collagenized stroma. To our knowledge, only a single case of oral lipidized FH affecting the tongue has been reported. We examine a case of lipidized FH in the buccal mucosa of a patient presenting with a gradually enlarging, pedunculated lesion measuring up to 26 mm. A histological examination revealed a well-marginated but unencapsulated tumor with a Grenz zone, hyalinized stroma, and central foam cell aggregation. Immunohistochemically, the spindle and foam cells were CD68-positive, with focal Factor XIIIa positivity and negative bcl-2 staining. The lesion was completely excised, and no recurrence was observed. To our knowledge, this is the second reported case of oral lipidized FH and the first case in the buccal mucosa. Given its rarity and histological overlap with other xanthomatous lesions, accurate diagnosis is crucial with immunohistochemistry. Complete excision appears to be curative; however, a long-term follow-up is recommended, considering the subtype of fibrous histiocytoma developing in the orofacial region. |
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AbstractList | Benign fibrous histiocytoma (FH) is a common cutaneous tumor that rarely occurs in the oral cavity. Lipidized FH is an uncommon variant characterized by abundant foam cells in collagenized stroma. To our knowledge, only a single case of oral lipidized FH affecting the tongue has been reported. We examine a case of lipidized FH in the buccal mucosa of a patient presenting with a gradually enlarging, pedunculated lesion measuring up to 26 mm. A histological examination revealed a well-marginated but unencapsulated tumor with a Grenz zone, hyalinized stroma, and central foam cell aggregation. Immunohistochemically, the spindle and foam cells were CD68-positive, with focal Factor XIIIa positivity and negative bcl-2 staining. The lesion was completely excised, and no recurrence was observed. To our knowledge, this is the second reported case of oral lipidized FH and the first case in the buccal mucosa. Given its rarity and histological overlap with other xanthomatous lesions, accurate diagnosis is crucial with immunohistochemistry. Complete excision appears to be curative; however, a long-term follow-up is recommended, considering the subtype of fibrous histiocytoma developing in the orofacial region.Benign fibrous histiocytoma (FH) is a common cutaneous tumor that rarely occurs in the oral cavity. Lipidized FH is an uncommon variant characterized by abundant foam cells in collagenized stroma. To our knowledge, only a single case of oral lipidized FH affecting the tongue has been reported. We examine a case of lipidized FH in the buccal mucosa of a patient presenting with a gradually enlarging, pedunculated lesion measuring up to 26 mm. A histological examination revealed a well-marginated but unencapsulated tumor with a Grenz zone, hyalinized stroma, and central foam cell aggregation. Immunohistochemically, the spindle and foam cells were CD68-positive, with focal Factor XIIIa positivity and negative bcl-2 staining. The lesion was completely excised, and no recurrence was observed. To our knowledge, this is the second reported case of oral lipidized FH and the first case in the buccal mucosa. Given its rarity and histological overlap with other xanthomatous lesions, accurate diagnosis is crucial with immunohistochemistry. Complete excision appears to be curative; however, a long-term follow-up is recommended, considering the subtype of fibrous histiocytoma developing in the orofacial region. Benign fibrous histiocytoma (FH) is a common cutaneous tumor that rarely occurs in the oral cavity. Lipidized FH is an uncommon variant characterized by abundant foam cells in collagenized stroma. To our knowledge, only a single case of oral lipidized FH affecting the tongue has been reported. We examine a case of lipidized FH in the buccal mucosa of a patient presenting with a gradually enlarging, pedunculated lesion measuring up to 26 mm. A histological examination revealed a well-marginated but unencapsulated tumor with a Grenz zone, hyalinized stroma, and central foam cell aggregation. Immunohistochemically, the spindle and foam cells were CD68-positive, with focal Factor XIIIa positivity and negative bcl-2 staining. The lesion was completely excised, and no recurrence was observed. To our knowledge, this is the second reported case of oral lipidized FH and the first case in the buccal mucosa. Given its rarity and histological overlap with other xanthomatous lesions, accurate diagnosis is crucial with immunohistochemistry. Complete excision appears to be curative; however, a long-term follow-up is recommended, considering the subtype of fibrous histiocytoma developing in the orofacial region. |
Author | Murakami, Satoshi Shimada, Katsumitsu Hasegawa, Hiromasa |
AuthorAffiliation | 3 Department of Oral Pathology/Forensic Odontology, School of Dentistry, Aichi Gakuin University, Nagoya, JPN 2 Hard Tissue Pathology Unit, Graduate School of Oral Medicine, Matsumoto Dental University, Shiojiri, JPN 1 Department of Clinical Pathophysiology, Matsumoto Dental University, Shiojiri, JPN |
AuthorAffiliation_xml | – name: 1 Department of Clinical Pathophysiology, Matsumoto Dental University, Shiojiri, JPN – name: 2 Hard Tissue Pathology Unit, Graduate School of Oral Medicine, Matsumoto Dental University, Shiojiri, JPN – name: 3 Department of Oral Pathology/Forensic Odontology, School of Dentistry, Aichi Gakuin University, Nagoya, JPN |
Author_xml | – sequence: 1 givenname: Katsumitsu surname: Shimada fullname: Shimada, Katsumitsu – sequence: 2 givenname: Satoshi surname: Murakami fullname: Murakami, Satoshi – sequence: 3 givenname: Hiromasa surname: Hasegawa fullname: Hasegawa, Hiromasa |
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Cites_doi | 10.1016/j.amjoto.2012.09.008 10.1590/abd1806-4841.20142629 10.1007/s12105-019-01123-0 10.1038/s41572-021-00307-9 10.3390/diagnostics13020185 10.1097/PAS.0b013e31827070d4 10.1038/modpathol.3880115 10.1097/DAD.0b013e31818981ff 10.1111/j.1365-2559.2009.03447.x 10.1034/j.1600-0560.2003.00126.x 10.1097/SCS.0000000000000911 10.1111/j.1600-0560.2008.01001.x 10.1097/00000372-200004000-00007 10.1097/DAD.0b013e31813735df 10.1097/00000372-200608000-00003 10.1097/DAD.0000000000002211 10.1016/j.oooo.2021.07.003 10.1111/cup.13512 10.3348/kjr.2005.6.1.22 10.1097/00000478-200210000-00007 10.1097/00000372-200110000-00006 10.5021/ad.2011.23.2.185 10.1007/s12663-015-0811-4 10.1016/s0046-8177(98)90275-1 10.1097/00000478-199807000-00008 10.1097/00000372-199410000-00015 10.1016/j.jds.2024.06.008 |
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Copyright | Copyright © 2025, Shimada et al. Copyright © 2025, Shimada et al. This is an open access article distributed under the terms of the Creative Commons Attribution License CC-BY 4.0., which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. Copyright © 2025, Shimada et al. 2025 Shimada et al. |
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Keywords | foam cells oral cavity cd68 factor xiiia lipidized fibrous histiocytoma |
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Title | A Rare Case of Lipidized Fibrous Histiocytoma of the Oral Cavity |
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