PMID- 28387003 OWN - NLM STAT- MEDLINE DCOM- 20180416 LR - 20180416 IS - 1365-2303 (Electronic) IS - 0956-5507 (Linking) VI - 28 IP - 4 DP - 2017 Aug TI - Cytomorphological changes induced by intraperitoneal chemotherapy present important diagnostic pitfalls in peritoneal fluid cytology. PG - 299-306 LID - 10.1111/cyt.12424 [doi] AB - OBJECTIVE: Intraperitoneal chemotherapy (IP ChT) is an emerging modality in the treatment of advanced gastric adenocarcinoma with peritoneal disease. Cytological evaluation of peritoneal fluid specimens from patients undergoing IP ChT is important in clinical management. However, direct intraperitoneal exposure to chemotherapeutic agents induces cytomorphological changes in benign constituents of peritoneal fluid, presenting particular challenges to accurate cytological interpretation. These morphological changes have not been well characterised in the literature. We systematically reviewed the cytomorphological features in immunocytochemically-confirmed positive and negative IP ChT peritoneal fluid samples to elucidate the degree of morphological overlap between malignant and reactive cells. METHODS: We reviewed 39 peritoneal fluid samples of patients treated with IP ChT, and scored specific cytomorphological parameters of both benign and malignant cells with the aid of relevant immunocytochemical interrogation. RESULTS: The present findings show a significant degree of morphological overlap between reactive and malignant cells. Abnormal, "exploding" mitotic figures, nuclear membrane irregularities, multi-nucleation and cytoplasmic vacuolation were commonly observed in negative fluid specimens. The most helpful feature that favoured malignant cells was the increased nuclear-to-cytoplasmic ratio. A background inflammatory milieu of eosinophils and/or neutrophils was seen in 45-58% of post IP ChT peritoneal fluid specimens. The presence of pseudoparakeratotic cells, a novel observation in post IP ChT fluid specimens is also described. CONCLUSIONS: The extent of reactive cytomorphological anomalies arising from treatment with IP ChT poses unique diagnostic challenges and may prompt a malignant or 'atypical' diagnosis in benign reactive samples. CI - (c) 2017 John Wiley & Sons Ltd. FAU - Mok, Y AU - Mok Y AUID- ORCID: 0000-0003-0151-2203 AD - Department of Pathology, National University Health System, Singapore, Singapore. FAU - Nga, M E AU - Nga ME AD - Department of Pathology, National University Health System, Singapore, Singapore. LA - eng PT - Journal Article DEP - 20170407 PL - England TA - Cytopathology JT - Cytopathology : official journal of the British Society for Clinical Cytology JID - 9010345 SB - IM MH - Ascitic Fluid/*pathology MH - Cell Nucleus/pathology MH - Cohort Studies MH - Cytodiagnosis/*methods MH - Humans MH - Immunohistochemistry MH - Inflammation/pathology MH - Injections, Intraperitoneal MH - Peritoneal Neoplasms/diagnosis/*drug therapy/pathology OTO - NOTNLM OT - cytology OT - gastric adenocarcinoma OT - intraperitoneal chemotherapy OT - peritoneal fluid EDAT- 2017/04/08 06:00 MHDA- 2018/04/17 06:00 CRDT- 2017/04/08 06:00 PHST- 2017/02/09 00:00 [accepted] PHST- 2017/04/08 06:00 [pubmed] PHST- 2018/04/17 06:00 [medline] PHST- 2017/04/08 06:00 [entrez] AID - 10.1111/cyt.12424 [doi] PST - ppublish SO - Cytopathology. 2017 Aug;28(4):299-306. doi: 10.1111/cyt.12424. Epub 2017 Apr 7.