J Pathol Transl Med.  2017 Jan;51(1):49-55. 10.4132/jptm.2016.09.19.

Diagnostic Significance of Cellular Neuroglial Tissue in Ovarian Immature Teratoma

Affiliations
  • 1Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. krkim@amc.seoul.kr
  • 2Department of Pathology, Soonchunhyang University Bucheon Hospital, Soonchunhyang University College of Medicine, Bucheon, Korea.
  • 3Department of Pathology, Korea University Anam Hospital, Korea University College of Medicine, Seoul, Korea.

Abstract

BACKGROUND
Immature teratoma (IT) is a tumor containing immature neuroectodermal tissue, primarily in the form of neuroepithelial tubules. However, the diagnosis of tumors containing only cellular neuroglial tissue (CNT) without distinct neuroepithelial tubules is often difficult, since the histological characteristics of immature neuroectodermal tissues remain unclear. Here, we examined the significance of CNT and tried to define immature neuroectodermal tissues by comparing the histological features of neuroglial tissues between mature teratoma (MT) and IT.
METHODS
The histological features of neuroglial tissue, including the cellularity, border between the neuroglial and adjacent tissues, cellular composition, mitotic index, Ki-67 proliferation rate, presence or absence of tissue necrosis, vascularity, and endothelial hyperplasia, were compared between 91 MT and 35 IT cases.
RESULTS
CNTs with a cellularity grade of ≥ 2 were observed in 96% of IT cases and 4% of MT cases (p < .001); however, CNT with a cellularity grade of 3 in MT cases was confined to the histologically distinct granular layer of mature cerebellar tissue. Moreover, CNT in IT exhibited significantly higher rates of Ki-67 proliferation, mitoses, and necrosis than those in MT (p < .001). Furthermore, an infiltrative border of neuroglial tissue and glomeruloid endothelial hyperplasia were significantly more frequent in IT cases than in MT cases (p < .001).
CONCLUSIONS
Our results suggest that if CNT with a cellularity grade of ≥ 2 is not a component of cerebellar tissue, such cases should be diagnosed as IT containing immature neuroectodermal tissue, particularly if they exhibit an infiltrative border, mitoses, necrosis, and increased Ki-67 proliferation.

Keyword

Immature teratoma; Neuroectodermal; Neuroglia; Neuroepithelium; Ki-67; Ovary

MeSH Terms

Diagnosis
Female
Hyperplasia
Mitosis
Mitotic Index
Necrosis
Neural Plate
Neuroglia
Ovary
Teratoma*

Figure

  • Fig. 1. Cellular neuroglial tissue. The diagnosis of immature teratoma containing only cellular neuroglial tissue without distinct neuroepithelial tubules is often difficult since the histological characteristics of immature neuroectodermal tissues have not been clearly defined.

  • Fig. 2. Cellularity of neuroglial tissue in mature and immature teratomas. (A) Grade 1 referred to cellularity comparable to that of normal white matter or an inter-nuclear distance longer than 5 nuclear diameters. (B, C) Grade 2 applied to cases with either heterogeneous cellularity or with inter-nuclear distances similar to 2–4 nuclear diameters. (D) Grade 3 cellularity referred to cellularity comparable to that of the germinal matrix of the fetal brain or the granular layer of the normal adult cerebellum wherein nuclei touch each other, or an inter-nuclear distance shorter than 1 nuclear diameter.

  • Fig. 3. Histopathologic Features Of Mature Teratoma And Immature Teratoma. Neuroglial Cells In A Mature Teratoma Show A Smooth Border (A), And Comprise Polymorphous Cellular Components (C). They Show No Mitotic Activity (E) And No Coagulative Necrosis (G), But Do Exhibit Focally Glomeruloid Endothelial Proliferation (I) And Rare Ki-67– Positive Proliferating Cells (K). In Contrast, Cellular Neuroglial Cells In Immature Teratoma Show An Infiltrative Border (B) More Frequently, And Comprise Monomorphic Germinal Matrix-like Cells (D). They Also Show Frequent Mitoses (F), Coagulative Necrosis (H), Glomeruloid Endothelial Proliferation (J), And Increased Ki-67–positive Proliferating Cells (L).


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