Medulloblastomas with extensive posttherapy neuronal maturation (original) (raw)
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Report of two cases
Dan X. Cai
Dan X. Cai Departments of Pathology and Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri; Department of Pathology, Hospital S. Jose, Lisbon, Portugal; and Department of Pathology/Laboratory Medicine, Mayo Clinic, Rochester, Minnesota
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Manuela Mafra
Manuela Mafra Departments of Pathology and Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri; Department of Pathology, Hospital S. Jose, Lisbon, Portugal; and Department of Pathology/Laboratory Medicine, Mayo Clinic, Rochester, Minnesota
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Robert E. Schmidt
Robert E. Schmidt Departments of Pathology and Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri; Department of Pathology, Hospital S. Jose, Lisbon, Portugal; and Department of Pathology/Laboratory Medicine, Mayo Clinic, Rochester, Minnesota
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Bernd W. Scheithauer
Bernd W. Scheithauer Departments of Pathology and Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri; Department of Pathology, Hospital S. Jose, Lisbon, Portugal; and Department of Pathology/Laboratory Medicine, Mayo Clinic, Rochester, Minnesota
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Tae Sung Park
Tae Sung Park Departments of Pathology and Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri; Department of Pathology, Hospital S. Jose, Lisbon, Portugal; and Department of Pathology/Laboratory Medicine, Mayo Clinic, Rochester, Minnesota
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Arie Perry
Arie Perry Departments of Pathology and Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri; Department of Pathology, Hospital S. Jose, Lisbon, Portugal; and Department of Pathology/Laboratory Medicine, Mayo Clinic, Rochester, Minnesota
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✓ The authors report on two patients with classic medulloblastoma, each of whom underwent extensive therapy-associated neuronal maturation. The first patient presented at 3 months of age with hydrocephalus caused by a 5-cm tumor in the cerebellar vermis. He underwent a gross-total resection of a desmoplastic medulloblastoma. No mature elements were identified. Despite adjuvant chemotherapy, a 1.5-cm recurrent tumor developed 6 months later. Sections from the subtotally resected tumor demonstrated exclusively mature neuronal elements, ranging from neurocytes to ganglion cells. Four months later, a second recurrent tumor was resected. The specimen collected this time demonstrated classic medulloblastoma morphological characteristics. The patient was subsequently treated with radiation therapy, which seemed to have an effect; however, the tumor eventually progressed and the patient died. The second patient presented at 3 years of age with a midline medulloblastoma and was treated with subtotal resection, radiation therapy, and chemotherapy. Although the tumor remained stable on radiographic imaging, a second resection was performed 8 years later to alleviate hydrocephalus. Histological examination revealed predominantly small mature neurons with scattered ganglion cells and extensive calcification. No adjuvant therapy was given and the patient is alive and well as of his last follow-up examination.
The mature neuronal neoplasms resected in both patients demonstrated negligible proliferative indices and stained appropriately with neuronal immunohistochemical markers. The smaller neuronal population resembled those of a central neurocytoma and medullocytoma/cerebellar neurocytoma. Analogous to neuroblastoma, our cases suggest that adjuvant therapy can induce extensive or complete neuronal maturation in medulloblastoma. Additional cases must be studied to determine the prognostic significance of this rare phenomenon.