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Case Summary: An 11-year-old female spayed domestic medium-hair cat presented for dental prophylaxis, at which time no oral mass was appreciated. Fifteen days after a dental cleaning, a mass expanding the oral mucosa of the rostral mandible was identified. An incisional biopsy revealed that the oral mucosa was infiltrated by neoplastic round-to-spindloid mesenchymal cells arranged in streams and small, dense aggregates consistent with an undifferentiated sarcoma. The patient was managed medically for approximately 6 months following the diagnosis, but, owing to declining health, euthanasia was elected and a post-mortem examination was performed. On post-mortem examination, the previously described neoplastic cells were infiltrating the rostral mandible and had metastasized to the right submandibular lymph node. Immunohistochemistry performed during the postmortem examination found that neoplastic cells were positive for Iba-1, CD18 and CD204, and negative for MUM-1, S100, Melan-A and E-cadherin, favoring a diagnosis of oral histiocytic sarcoma. Although recently recognized in cats, feline oral histiocytic sarcoma is rare, the tumor's immunohistochemical profile is unstandardized, and the tumor's behavior and prognosis are unclear. The diagnosis is challenging if small incisional biopsies are submitted and the neoplasm is poorly differentiated. This case report discusses the clinical, macroscopic, microscopic and immunohistochemical features of oral histiocytic sarcoma in a cat with mandibular invasion and submandibular lymph node metastasis.
Relevance And Novel Information: Feline primary oral histiocytic sarcoma is rare and tumor behavior and prognosis are unclear. This report broadens the immunohistochemical features of the tumor and recognizes mandibular invasion and submandibular lymph node metastasis.
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http://dx.doi.org/10.1177/20551169211058044 | DOI Listing |
BMJ Case Rep
July 2025
Department of Radiology, Instituto Português de Oncologia de Lisboa Francisco Gentil EPE, Lisboa, Portugal
We describe the case of a young adult woman presenting with progressive bilateral proptosis, periorbital soft tissue swelling and eyelid skin lesions. Imaging showed thickened eyelids and enlarged lacrimal glands and extraocular muscles, and a biopsy of the eyelid disclosed a xanthogranulomatous lesion with increased IgG4+ plasma cells. Further investigation did not reveal any associated systemic findings, and the diagnosis of adult-onset xanthogranuloma was made.
View Article and Find Full Text PDFHead Neck Pathol
July 2025
Joint Pathology Center, 606 Stephen Sitter Ave, Silver Spring, MD, 20910-1290, USA.
Background: BCM is an uncommon cytomorphologic variant with the potential to mimic unrelated neoplastic conditions, especially in the absence of a known cutaneous primary lesion or limited access to immunohistochemical stains.
Case Presentation: A 28-year-old male patient presented with recent onset parotid gland mass. The mass was excised, and the subsequent workup elicited an interpretation of metastatic balloon cell melanoma (BCM).
Cureus
June 2025
Department of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine, University of Toyama, Toyama, JPN.
Rosai-Dorfman disease (RDD) is a rare histiocytic disorder characterized by massive lymphadenopathy and, in some cases, extranodal involvement, resulting in significant functional impairment. Maxillary sinus lesions with orbital extension are extremely rare and may mimic malignancy. We report the case of a 76-year-old man who presented with left lower eyelid swelling and diplopia.
View Article and Find Full Text PDFBMC Pediatr
July 2025
Department of Infectious Diseases, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, National Center for Children's Infectious and Allergic Diseases Surveillance, Beijing Research Center for Respiratory Infectious Diseases, Beijing Key Laboratory of Core
Background: This study was performed to summarize the clinical and laboratory features of children with Kikuchi-Fujimoto disease (KFD). The risk factors of KFD recurrence were analyzed.
Methods: A retrospective case-control study was conducted on children who underwent lymph node biopsy in the department of infectious diseases of Beijing Children's Hospital from April 2018 to April 2022.
Cureus
May 2025
Medical Oncology, Gibbs Cancer Center, Spartanburg Regional Healthcare System, Spartanburg, USA.
Non-Langerhans cell histiocytosis (NLCH) is a broad disorder encompassing different diseases arising from dermal dendritic histiocytes. Xanthogranuloma (XG) is a cutaneous subtype of NLCH that can be present in isolated or multiple locations. If localized, XGs can be treated with surgical resection or radiation; however, if they present more disseminated, they are poorly responsive to traditional chemotherapeutic agents.
View Article and Find Full Text PDF