Rationale: Inflammatory pseudotumor-like follicular dendritic cell sarcoma (IPT-like FDCS) of the liver is rare. It was previously believed that Epstein-Barr virus (EBV) positivity was a necessary criterion for pathological diagnosis. However, we found that there were also cases of EBV negativity. Therefore, clinicians and pathologists are reminded that EBV positivity is not a necessary condition for diagnosis.

Patient Concerns: A 70-year-old female underwent computed tomography (CT) examination for upper abdominal discomfort, which revealed the presence of a liver tumor. Follow-up revealed that the tumor had progressively increased in size.

Diagnosis: The final diagnosis was an IPT-like follicular cell sarcoma, based on CT, MRI, HE staining, and immunohistochemical staining.

Interventions: The patient underwent a laparoscopic left hemihepatectomy.

Outcomes: The patient has not undergone any special treatment, such as radiotherapy and chemotherapy, and has been followed up for over 3 years without experiencing any recurrence.

Lessons: IPT-like FDCS is a rare tumor that lacks definitive criteria, and its diagnosis mainly relies on pathological findings. Previously, it was believed that being EBV-positive was an important condition for diagnosis. Primary IPT-like FDCS in the liver is even rarer, and the patient in this case tested negative for EBV. It may be necessary for pathologists to consider the role of EBV in the diagnosis of IPT-like FDCS.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10994431PMC
http://dx.doi.org/10.1097/MD.0000000000037651DOI Listing

Publication Analysis

Top Keywords

ipt-like fdcs
16
cell sarcoma
12
inflammatory pseudotumor-like
8
pseudotumor-like follicular
8
follicular dendritic
8
dendritic cell
8
fdcs liver
8
ebv positivity
8
diagnosis ipt-like
8
ipt-like
5

Similar Publications

Objective: This study aimed to outline the computed tomography (CT) and magnetic resonance imaging (MRI) characteristics of inflammatory pseudotumor-like follicular dendritic cell sarcoma (IPT-like FDCS) in the spleen and to link these imaging features with histopathological findings.

Materials And Methods: A retrospective analysis was conducted on 11 patients (3 males, 8 females; mean age, 63.3 ± 9.

View Article and Find Full Text PDF
Article Synopsis
  • Follicular dendritic cell sarcoma (FDCS) is a rare cancer type, with a specific variant called inflammatory pseudotumor-like FDCS (IPT-like FDCS) having very few established treatment protocols due to its low incidence.
  • A case study presented here involved a patient with EBV-positive IPT-like FDCS, initially presenting with thrombocytopenia, for which splenectomy was performed, leading to no signs of recurrence during a one-year follow-up.
  • Analysis of 30 cases revealed a slight female predominance, a median age of 62, diverse symptoms, and consistent findings of EBV positivity, with surgical treatment being the common approach for all patients.
View Article and Find Full Text PDF

Inflammatory pseudotumor-like follicular dendritic cell sarcoma (IPT-like FDCS) is a rare malignancy with fewer than 150 cases in the literature. IPT-like FDCS follows an indolent course with most cases definitively managed with surgical resection. We present a case of IPT-like FDCS with multiple recurrences with a trial of immunotherapy.

View Article and Find Full Text PDF

Rationale: Inflammatory pseudotumor-like follicular dendritic cell sarcoma (IPT-like FDCS) of the liver is rare. It was previously believed that Epstein-Barr virus (EBV) positivity was a necessary criterion for pathological diagnosis. However, we found that there were also cases of EBV negativity.

View Article and Find Full Text PDF

: Follicular dendritic cell (FDC) sarcoma is an uncommon mesenchymal origin neoplasm derived from the abnormal proliferation and differentiation of FDCs. Epstein‒Barr virus-positive inflammatory follicular dendritic cell sarcoma (EBV+ iFDCS), which used to be known as the inflammatory pseudotumour (IPT)-like variant, occurs exclusively in the liver and spleen and has rarely been reported in the gastrointestinal tract. : Here, we report a case of a 52-year-old woman with a special family history undergoing a routine physical examination.

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!