1.Hemophilic pseudotumor of the ulna treated with low dose radiation therapy: a case report.
Jin Oh KANG ; Yoon Je CHO ; Myung Chul YOO ; Seong Eon HONG
Journal of Korean Medical Science 2000;15(5):601-603
We report a case of hemophilic pseudotumor in the ulna of a 6-year-old boy treated with radiation therapy. A total dose of 900 cGy in 6 fractions was given in 6 consecutive days. Progression of cystic changes was halted within a month. New bone formation and trabeculation were found on the 4th month. Complete healing of the lesion and bony replacement were found on the 12th month. The patient was followed up to 72 months and there was no evidence of recurrence and no bone growth disturbance. Radiation therapy can be an effective alternative modality in treating hemophilic pseudotumor.
Bone Cysts/radiotherapy*
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Bone Cysts/pathology
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Bone Cysts/etiology*
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Case Report
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Child
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Hemophilia A/pathology
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Hemophilia A/complications*
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Human
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Male
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Ulna/pathology*
2.Malignant Ectomesenchymoma in a Two-Month-Old Boy.
Ji Young HWANG ; Ji Hyoun SEO ; Jeum Su KIM ; Young Suk KIM ; Sue Jin LEE ; Chan Hoo PARK ; Yoo Kyung KIM ; Sun Hoo PARK ; Jung Hee LEE ; In Oak AHN ; Ki Hyun CHUNG ; Byung Kiu PARK
Journal of the Korean Pediatric Society 2001;44(8):959-964
Malignant ectomesenchymoma is a rare tumor originating from remnants of migratory neural crest(ectomesenchyme) and composed of neuroectodermal as well as mesenchymal components. Neuroblasts and ganglion cells constitute the neuroectodermal components and rhabdomyosarcoma is the most frequently encountered mesenchymal components. We report a case of malignant ectomesenchymoma in a two-month-old boy who was presented with abdominal pain and urinary difficulty. The tumor appeared to arise from the prostatic region and enlarged to compress the bladder leading to bilateral hydronephrosis. Immunohistochemical studies for the resected tumor confirmed the presence of mixed ganglioneuroma and rhabdomyosarcoma establishing the diagnosis of malignant ectomesenchymoma. However, in the initial biopsy specimen of tumor, poorly differentiated round to oval cells positive for both desmin and vimentin staining were uniformly noted and the incorrect diagnosis of rhabdomyosarcoma was made. Intensive multi-agents chemotherapy, surgery and radiotherapy had failed in preventing the development of local recurrences. Subsequently, invasion of pubic bone and lung metastases ensued. This report enlightens the need for immunohistochemistry to seek possible neuroectodermal components in a tumor specimen suggestive of rhabdomyosarcoma.
Abdominal Pain
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Biopsy
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Desmin
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Diagnosis
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Drug Therapy
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Ganglion Cysts
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Ganglioneuroma
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Humans
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Hydronephrosis
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Immunohistochemistry
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Lung
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Male*
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Neoplasm Metastasis
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Neural Plate
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Pubic Bone
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Radiotherapy
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Recurrence
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Rhabdomyosarcoma
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Urinary Bladder
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Vimentin