- Lhermitte-Duclos Disease in a Sudden Death: An autopsy case.
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Tae Jung Kwon, Tae Seung Kim, Han Young Lee, Shin Mong Kang
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Korean J Pathol. 1994;28(1):73-78.
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 Abstract
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- Lhermitte-Duclos disease of the cerebellum manifests itself as a slowly growing mass formed by abnormal neurons that appear more malformative than tumoral. Although most cases show satisfactory clinical evolution, several cases, not recognized in life, died abruptly, usually from respiratory arrest. We recently experienced a 19 year old male, who died suddenly during alcohol drinking. At autopsy, the cerebellum revealed thickening of the folia over two limited areas.
Microscopically, the lesion was characterized by proliferation of abnormal neuronal cells with excessive myelination of their axons, disappearance of Purkinie cells and greatly reduced white mater. Theories regarding the pathogenesis of Lhermitte-Duclos disease were reviewed and discussed.
- Ovarian Paragonimiasis: A case report.
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Shin Mong Kang, Yong Koo Park, Ju Hie Lee, Jung Eun Mok, Moon Ho Yang
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Korean J Pathol. 1988;22(3):336-339.
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- The authors report a case of ectopic paragonimiasis in a 33 year old Korean housewife who came to the hospital because of lower abdominal discomfortness and palpable mass.
Parasitic granulomas involved the ovary and posterior wall of the uterine body. This report deals with the rare occurrence of a parasitic infestation in the ovary.
- Multicystic Renal Dysplasia associated with Ectopic Ureteral Orifice.
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Shin Mong Kang, Yong Koo Park, Ju Hie Lee, Soo Eung Chai, Moon Ho Yang
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Korean J Pathol. 1988;22(3):331-335.
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- A case of unilateral multicystic renal dysplasia was reported in view of rarity, and a review of literature 23-year-old female was admitted to Kyung Hee University Hospital with a complaint of urinary incontinence. An excretory urogram revealed non-visualization of the right kidney. The right ureter had opening at the 2 cm above the vaginal introitus. The resected right kidney revelaed multilobulated outer surface with multiloculated cystic struture on cut surface. The associated anomaly was uterine didelphy. The condition was treated by nephroureterectomy.
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