BACKGROUND
Neurocysticercosis (NCC), caused by the larval stage ofTaenia solium ( T solium ), is the most common and serious parasitic disease of the central nervous system (CNS) in the majority of developing countries where people eat pork. 1 2 Clinical manifestations of NCC are highly variable depending on the number, type, size, localisation and developmental stage of cysticerci with the host immune response. 3 NCC, echinococcosis, anthrax and rabies are now recognised as re-emerging, but neglected, infectious diseases worldwide. 2 4 If NCC is suspected through neuroimaging, either typical or atypical, and questionnaire on visiting and/or living history in endemic areas of T solium , it is strongly recommended to carry out serology using highly specifi c antigens. 2 5 -7 NCC cases with multiple cysts are rather easily detectable by such a serology. 2 However, even highly specifi c serology is not always 100% sensitive especially in cases with solitary cyst, with calcifi ed cysts only or with background of immunodefi ciency. 2 Without typical neuroimaging or serological confi rmation of NCC, patients are often reluctantly treated surgically with suspected diagnosis of malignant tumours, tuberculosis or any other diseases causing neurological disorders especially in non-endemic countries. 2 Therefore, pathological approaches on NCC cases could inevitably become feasible for crucial diagnosis to identify such NCC cases. It is not always easy that the infectious diseases including atypical NCC are confi rmed with the surgical specimens of the brain in non-endemic countries. However, molecular diagnosis using PCR has been introduced and established for molecular diagnosis of many pathogens and provided satisfactory results in NCC as well. 8 -11
CASE PRESENTATIONAn Indian woman was referred to our hospital for the evaluation of multiple and nodular cerebral lesions. Two months before admission to our hospital, she noted occasional headache and paraesthesia of right forearm and MRI, examined in a local hospital, revealed Gd-well enhanced multiple nodular lesions with peripheral oedema and scattered calcifi cations ( fi gure 1 ). Because no neoplastic lesions could be excluded on the basis of these radiological fi ndings and because NCC is not indigenous in Japan 1 2 and most of clinicians have no or poor knowledge on NCC without their own experiences, NCC unfortunately was not suspected as a causative disease, and a brain biopsy was performed in a local hospital. However, fi gure 2 strongly suggested somewhat typical image of NCC with oedema, and if the clinicians tried to get second opinions from parasitologists, chemotherapy without neurosurgery could strongly be recommended with sound serological evidence. 1 2 6 12 The H&E-stained microsections derived from one of the cerebral nodules showed presence of epithelioid granulomas surrounded by reactive gliosis ( fi gure 3A ). These granulomas were also divided into three layers including plasma cell-rich mononuclear cell outer layer (mo), epithelioid-cell middl...