1.Paediatric Primary Pachymeningeal Xanthogranuloma with Scattered Foci Displaying Reticulohistiocytoma-like Features.
Miguel Fdo SALAZAR ; Maria del Rocio ESTRADA HERNANDEZ ; Erick GOMEZ APO ; Laura G CHAVEZ MACIAS ; Carlos Alfonso RODRIGUEZ ALVAREZ
Journal of Pathology and Translational Medicine 2015;49(5):403-408
We report a unique case of a 4-year-old girl with an intriguing fibrohistiocytic tumour. Magnetic resonance imaging scans showed a dural mass of variegated intensity compressing the left occipital pole and apparently extending toward the superior sagittal sinus. Grossly, the cut surface of the surgical specimen was yellow, pale, and soft with reddish kernel-like crusts. Histologically, the yellow areas resembled cholesterol granulomas with widespread coagulative necrosis, cholesterol clefts, powdery calcification, foreign body-type giant cells, and foamy macrophages, while the scattered red spots contained numerous multinucleated giant cells of foreign-body and Touton types, the former with amphophilic to slightly eosinophilic cytoplasm. Immunoperoxidase reactions confirmed the expression of histiocytic markers and vimentin. As far as we know, no tumour displaying these peculiar morphological features has yet been described.
Child, Preschool
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Cholesterol
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Cytoplasm
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Eosinophils
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Female
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Giant Cells
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Giant Cells, Foreign-Body
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Granuloma
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Humans
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Macrophages
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Magnetic Resonance Imaging
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Necrosis
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Superior Sagittal Sinus
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Vimentin
2.Erratum: WHO Grade IV Gliofibroma: A Grading Label Denoting Malignancy for an Otherwise Commonly Misinterpreted Neoplasm.
Paola A ESCALANTE ABRIL ; Miguel Fdo SALAZAR ; Nubia L LOPEZ GARCIA ; Monica N MADRAZO MOYA ; Yadir U ZAMORA GUERRA ; Yadira Gandhi MATA MENDOZA ; Erick GOMEZ APO ; Laura G CHAVEZ MACIAS
Journal of Pathology and Translational Medicine 2015;49(6):538-538
We found errors in our published article.
3.WHO Grade IV Gliofibroma: A Grading Label Denoting Malignancy for an Otherwise Commonly Misinterpreted Neoplasm.
Paola A ESCALANTE ABRIL ; Miguel Fdo SALAZAR ; Nubia L LOPEZ GARCIA ; Monica N MADRAZO MOYA ; Yadir U ZAMORA GUERRA ; Yadira Gandhi MATA MENDOZA ; Erick GOMEZ APO ; Laura G CHAVEZ MACIAS
Journal of Pathology and Translational Medicine 2015;49(4):325-330
We report a 50-year-old woman with no relevant clinical history who presented with headache and loss of memory. Magnetic resonance imaging showed a left parieto-temporal mass with annular enhancement after contrast media administration, rendering a radiological diagnosis of high-grade astrocytic neoplasm. Tumour sampling was performed but the patient ultimately died as a result of disease. Microscopically, the lesion had areas of glioblastoma mixed with a benign mesenchymal constituent; the former showed hypercellularity, endothelial proliferation, high mitotic activity and necrosis, while the latter showed fascicles of long spindle cells surrounded by collagen and reticulin fibers. With approximately 40 previously reported cases, gliofibroma is a rare neoplasm defined as either glio-desmoplastic or glial/benign mesenchymal. As shown in our case, its prognosis is apparently determined by the degree of anaplasia of the glial component.
Anaplasia
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Collagen
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Contrast Media
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Diagnosis
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Female
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Glioblastoma
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Headache
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Humans
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Magnetic Resonance Imaging
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Memory
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Middle Aged
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Necrosis
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Prognosis
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Reticulin