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Neurology

Publication date: 2007-03-01
Volume: 68 Pages: 900 - 905
Publisher: Lippincott williams & wilkins

Author:

Mathew, RM
Vandenberghe, Rik ; Garcia-Merino, A ; Yamamoto, T ; Landolfi, JC ; Rosenfeld, MR ; Rossi, JE ; Thiessen, B ; Dropcho, EJ ; Dalmau, J

Keywords:

testicular intraepithelial neoplasia, germ-cell neoplasia, nervous-system, cancer, testis, microlithiasis, oct4, association, prevalence, diagnosis, Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, GERM-CELL NEOPLASIA, TESTICULAR INTRAEPITHELIAL NEOPLASIA, MICROLITHIASIS, CANCER, OCT4, PREVALENCE, DIAGNOSIS, BIOPSIES, TESTIS, TISSUE, Adult, Antigens, Neoplasm, Autoantibodies, Biomarkers, Tumor, Brain, Diagnosis, Differential, Early Diagnosis, Humans, Limbic Encephalitis, Magnetic Resonance Imaging, Male, Neoplasms, Germ Cell and Embryonal, Nerve Tissue Proteins, Neural Pathways, Orchiectomy, Predictive Value of Tests, Testicular Neoplasms, 1103 Clinical Sciences, 1109 Neurosciences, 1702 Cognitive Sciences, Neurology & Neurosurgery, 3202 Clinical sciences, 3209 Neurosciences

Abstract:

Abstract-- OBJECTIVE: To report the presence of microscopic neoplasms of the testis in men with anti-Ma2-associated encephalitis (Ma2-encephalitis) and to discuss the clinical implications. METHODS: Orchiectomy specimens were examined using immunohistochemistry with Ma2 and Oct4 antibodies. RESULTS: Among 25 patients with Ma2-encephalitis younger than 50 years, 19 had germ-cell tumors, and 6 had no evidence of cancer. These 6 patients underwent orchiectomy because they fulfilled five criteria: 1) demonstration of anti-Ma2 antibodies in association with MRI or clinical features compatible with Ma2-encephalitis, 2) life-threatening or progressive neurologic deficits, 3) age < 50 years, 4) absence of other tumors, and 5) new testicular enlargement or risk factors for germ-cell tumors, mainly cryptorchidism or ultrasound evidence of testicular microcalcifications. All orchiectomy specimens showed intratubular-germ cell neoplasms unclassified type (IGCNU) and other abnormalities including microcalcifications, atrophy, fibrosis, inflammatory infiltrates, or hypospermatogenesis. Ma2 was expressed by neoplastic cells in three of three patients examined. Even though most patients had severe neurologic deficits at the time of orchiectomy (median progression of symptoms, 10 months), 4 had partial improvement and prolonged stabilization (8 to 84 months, median 22.5 months) and two did not improve after the procedure. CONCLUSIONS: In young men with Ma2-encephalitis, 1) the disorder should be attributed to a germ-cell neoplasm of the testis unless another Ma2-expressing tumor is found, 2) negative tumor markers, ultrasound, body CT, or PET do not exclude an intratubular germ-cell neoplasm of the testis, and 3) if no tumor is found, the presence of the five indicated criteria should prompt consideration of orchiectomy.