[P-18] Solitary fibrous tumour of the prostate: a rare mesenchymal neoplasm – a case report
Solitary fibrous tumour (SFT) is an uncommon myofibroblastic tumour generally affecting the pleura. Differential diagnosis includes poorly differentiated adenocarcinoma and various mesenchymal neoplasm of prostate....
[P-17] Primary malignant melanoma of the lung: a case report of a very rare neoplasm occurring in young patient
Primary malignant melanoma of the lung (PMML) is rare, with limited published reports. This case report discussed the diagnosis and management of a PMML occurring in a young patient and reviewed existing literature....
[P-16] Characterisation of genomic alteration of FGFR3 by integrating analysis of the Cancer Genome Atlas
Mutations and fusions of the fibroblast growth factor receptor (FGFR) gene family occur in various cancer types. Recently erdafitinib has been approved by the FDA for the treatment of FGFR3-altered urothelial cancer. We performed an integrated analysis of the TCGA-pancancer atlas including 32 cancer types (n = 10,953) to reveal the novel alteration of FGFR3....
[P-15] Paediatric gastric adenocarcinoma: two case reports and literature review
Paediatric gastric adenocarcinoma (GAC) is an extremely rare with limited relevant data. Until now, the clinical presentation and outcome have not yet been thoroughly understood....
[P-14] Post-chemotherapy histiocyte-rich pseudotumour involving the pancreas
Histiocyte-rich pseudotumour (HPRT) developing post-chemoradiation therapy is a rare benign reaction. Although benign, it can clinically and radiologically mimic residual tumours or recurrent/relapsed disease, causing challenges in management....
[P-13] Malignant pigmented epithelioid angiomyolipoma of the kidney in a child with tuberous sclerosis: a rare case report and literature review
Pigmented epithelioid angiomyolipoma is a rare variant of epithelioid Angiomyolipoma (EAML), a part of the family of the perivascular epithelioid cell neoplasms (PEComas) with malignant potential. We reported one case of EAML occurring in the paediatric age group....
[P-12] Integrating analysis of the expression of IDO1 and TDO2 in bladder cancer
Several lines of evidence have been focused on the roles of tryptophan metabolism genes like indoleamine 2,3-dioxygenase 1 (IDO1) and tryptophan 2,3-dioxygenase (TDO2) in bladder cancer progression. However, the alternative way of targeting in cancer immunotherapy has been not yet investigated in bladder cancer....
[P-11] Haemangiopericytoma of the pineal region: report of a rare case in unusual location
Intracranial hemangiopericytoma (HPC) is a rare non-meningothelial mesenchymal tumour which derives from malignant transformation of pericytes. It has been accounting for 0.4% of all intracranial tumours. Primary HPC in the pineal region has been rarely reported. Here we report a rare case of the pineal HPC....
[P-10] Subcutaneous panniculitis-like T-cell lymphoma in paediatric population: a report of two cases and literature review
Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare entity of mature αβ cytotoxic T-cells commonly found in young adults. We reported two cases of SPTCL occurring in the paediatric age group....
[P-09] Metastasis of primary breast undifferentiated pleomorphic sarcoma to the lung mimicking adenocarcinoma on cytology: a case report
Undifferentiated pleomorphic sarcoma (UPS) constitutes less than of all sarcomas in adults. UPS dissemination usually occurs haematogenously, lungs are the primary organs for metastasis. We herein present a patient with UPS of the breast with lung metastases after 12 years. Cytological diagnosis mass in the lung is extremely challenging because it is mimicking primary adenocarcinoma of the lung....
