Primitive neuroectodermal tumor of the uterus - A case report

Citation
Bs. Ward et al., Primitive neuroectodermal tumor of the uterus - A case report, ACT CYTOL, 44(4), 2000, pp. 667-672
Citations number
42
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Journal title
ACTA CYTOLOGICA
ISSN journal
00015547 → ACNP
Volume
44
Issue
4
Year of publication
2000
Pages
667 - 672
Database
ISI
SICI code
0001-5547(200007/08)44:4<667:PNTOTU>2.0.ZU;2-R
Abstract
BACKGROUND: Primitive neuroectodermal tumor (PNET) is a rare tumor derived from fetal neuroectodermal cells. These tumors occur in the central nervous system and in peripheral locations. Histologic diagnosis is the standard s ince most of these tumors are detected at an advanced stage. CASE: A 17-year-old female presented with persistent vaginal bleeding. Phys ical examination revealed a 4-cm, hard, barrel-shaped cervix. A cervicovagi nal smear was obtained. The specimen was hypercellular, with small to mediu m-sized, round, malignant cells. A diagnosis of PNET was made from the hist ologic sections of the surgical specimen. CONCLUSION: When numerous small round cells in a diffuse pattern are seen o n a Pap? smear, the differential diagnosis is long and difficult. However, with careful evaluation of the cytologic features, a few reasonable differe ntial diagnoses can be reached. Furthermore, with liquid-based Pap smears, material is available for immunohistochemical staining to narrow the range even more. Using all resources, including a good clinical history, a cytopa thologist can give the clinician an early diagnosis for intervention and tr eatment.