A case of nasal polyposis with stroma cell atypia in a 33-year-old man is reported. The light microscopic appearance made a rhabdomyosarcoma strongly suspected because of the presence of polymorphous, acidophilic, rhabdomyoblast-like cells. The clinical course was that of an ordinary recurring inflammatory nasal polyp. The ultrastructural and immunohistochemical analysis showed the fibroblastic and histiocytic nature of the atypical cells as being of a probably reactive nature. The reported case illustrates the value of electron microscopy and immunohistochemistry in the evaluation of the true type and nature of atypical mesenchymal cells in pseudosarcomatous lesions.

Download full-text PDF

Source

Publication Analysis

Top Keywords

cells pseudosarcomatous
8
type nature
8
mesenchymal cells
8
nature atypical
8
cells
5
nasal polyps
4
polyps atypical
4
atypical stroma
4
stroma cells
4
pseudosarcomatous lesion
4

Similar Publications

Reactive spindle cell nodules (RSCNs) that occur after fine needle aspiration (FNA) are commonly documented in the literature. They are benign proliferation of spindle cells with some mitotic figures and nuclear pleomorphism that arise after tissue injuries like FNA. These lesions are non-capsulated and surrounded by parenchyma of organ tissue.

View Article and Find Full Text PDF

Ischemic fasciitis in a mobile elderly patient: A case report.

Exp Ther Med

December 2024

Department of Pathology and Laboratory Medicine, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

Ischemic fasciitis (IF) is a rare pseudosarcomatous lesion usually occurring in physically debilitated or immobilized, elderly patients. The current case presents a 76-year-old mobile man with IF on his back. The 33-mm subcutaneous lesion, focally involving the latissimus dorsi muscle, had been slowly increasing in size for 2 months and was clinically suggested to be a soft-tissue sarcoma.

View Article and Find Full Text PDF

Inflammatory myofibroblastic tumor of the urinary bladder with FN1‑ALK gene fusion: A case report.

Oncol Lett

June 2023

Department of Pathology, Chungbuk National University Hospital, Chungbuk National University College of Medicine, Cheongju, North Chungcheong 28644, Republic of Korea.

Article Synopsis
  • A case report describes a 45-year-old woman diagnosed with an IMT in her bladder, presenting with symptoms like gross hematuria, and subsequent analysis revealed the FN1-ALK fusion after tumor resection.
  • The study indicates that the FN1-ALK fusion, involving ALK exon 19 and FN1 exon 23, is primarily associated with urinary bladder IMTs, distinguishing it from other IMTs that usually involve different ALK exons.
View Article and Find Full Text PDF
Article Synopsis
  • - The study aimed to explore the features and diagnosis of cranial fasciitis (CF), focusing on its clinical presentation, imaging methods, and genetic changes by analyzing clinical and pathologic data from 19 cases.
  • - The cases involved a majority of young patients (average age 29 months) with painless, rapidly growing masses affecting various skull regions, which did not show recurrence or metastasis post-surgery.
  • - Histological findings revealed spindle-shaped fibroblasts with specific immunohistochemical markers, and USP6 gene abnormalities were found in approximately 10.52% of cases, indicating that CF is a benign condition but challenging to diagnose prior to surgery.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!