Journal of Global Infectious Diseases

: 2010  |  Volume : 2  |  Issue : 3  |  Page : 313--314

Multiple-ring enhancing lesions in an immunocompetent adult

Amit Agrawal1, Arvind Bhake2, VM Sangole2, Brij R Singh3,  
1 Professor in Neurosurgery, Department of Neurosurgery, Datta Meghe Institute of Medical Sciences, Sawangi (Meghe), Wardha, India
2 Professor in Pathology, Department of Pathology, Datta Meghe Institute of Medical Sciences, Sawangi (Meghe), Wardha, India
3 Assistant Lecturer in Radiology, Department of Radiology, Datta Meghe Institute of Medical Sciences, Sawangi (Meghe), Wardha, India

Correspondence Address:
Amit Agrawal
Professor in Neurosurgery, Department of Neurosurgery, Datta Meghe Institute of Medical Sciences, Sawangi (Meghe), Wardha

How to cite this article:
Agrawal A, Bhake A, Sangole V M, Singh BR. Multiple-ring enhancing lesions in an immunocompetent adult.J Global Infect Dis 2010;2:313-314

How to cite this URL:
Agrawal A, Bhake A, Sangole V M, Singh BR. Multiple-ring enhancing lesions in an immunocompetent adult. J Global Infect Dis [serial online] 2010 [cited 2022 Sep 27 ];2:313-314
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Toxoplasma gondii (an intracellular coccidian parasite) is the most common cause of protozoon infections in humans and is highly prevalent in the adult population in the world and demonstrates various clinical manifestations throughout the world. [1],[2],[3] A 25-year-old gentleman was a known case of seizure disorders for the last 8 months and was receiving anticonvulsants regularly. He was diagnosed as having a right frontal ring enhancing lesion, a positive Mantoux test (14 Χ 15 mm with erythema) and a raised erythrocyte sedimentation rate (18 mm in the first hour). There was no history of loss of appetite, loss of weight and lack of energy or history of alcohol addiction or blood transfusion. General physical examination, including abdominal examination and pulmonary and cardiac examinations was normal. There was no lymphadenopathy. Based on imaging findings and laboratory findings in an endemic setting of a developing country, a diagnosis of cerebral tuberculoma was suspected and the patient was started on anticonvulsants and antitubercular treatment at a peripheral hospital. However, the follow-up magnetic resonance imaging (MRI) scan showed that the lesion was persistent and there was appearance of new lesions. MR spectroscopy showed significant elevation of lipid peak with decreased N-acetyl aspartate (NAA) choline and creatinine peak. Human immunodeficiency virus (HIV) was nonreactive on enzyme-linked immunosorbent assay (ELISA). Liver function was normal. On MRI, there were multiple thick wall ring enhancing lesions in bilateral frontal lobes. The largest one was seen in the right frontal lobe, measuring 2.4 x 2.0 x 2.4 cm in the subcortical location with significant perilesional vasogenic edema. On the left side, the lesions were cortical based, which were symmetrical in size. On T2/ Fluid attenuated-inversion-recovery (FLAIR), the lesions were hypointense with central hyperintensity signal. None of the lesions showed restriction of diffusion on DWI sequence. Single multivoxel MR spectroscopy in the right frontal lobe lesion at TE 35/144 showed significant elevation of lipid peak with a decrease in NAA choline and creatinine peaks [Figure 1]. All these findings were suggestive of likely infective disease. Following these findings, a diagnosis of neurocysticercosis was also suspected and Tab Albendazole was added. The patient was investigated for the immunocompromised state and the serological tests for HIV were negative. Also, ELISA for anticysticercosis antibodies and polymerase chain reaction for Mycobacterium tuberculosis antigen were negative. His chest X-ray and electrocardiography were normal. A repeat contrast MRI after 9 months showed the persistence of all the lesions and the patient was referred for a biopsy of the lesions. The patient underwent right frontal craniotomy and excision of the right frontal lesion. During surgery, there was well-defined firm, thick-walled lesion containing thick yellowish material. Histopathological examination of the specimen showed thick wall abscess and necrotic tissue with inflammatory cells in the center, features suggestive of toxoplasma cerebral abscess [Figure 2]. Further history of the patient revealed that there were many cats near his residence. The patient was started on appropriate treatment and was doing well at follow-up. Human infection is usually oligosymptomatic in immunocompetent individuals and the disease is considered to be self-limited and does not require treatment. [1],[3],[4] Severe acute disseminated toxoplasmosis has been rarely described in immunocompetent patients and, [5],[6] occasionally in normal patients, wherein they can develop long-lasting symptoms. [7],[8] The most common histological finding of toxoplasma abscess is nonspecific coagulative necrosis without toxoplasmic cysts. [1],[9] Although the gross pathology of a cerebral toxoplasmic abscess may resemble a pyogenic abscess, there are distinct histopathologic differences between the pyogenic and toxoplasma abscesses. When toxoplasmosis invades the brain, particularly in an immunocompromised patient, there is central necrosis with variable petechial hemorrhage that may become encircled by a ring of free tachyzoites, encysted bradyzoites and inflammatory cells. [11] As in the present case, the core of a toxoplasma abscess consists primarily of necrotic tissue and does not have the viscous, proteinaceous and inflammatory debris as seen in pyogenic abscess. [11] On imaging, the differential diagnosis of a rim-enhancing toxoplasma abscess include a primary or metastatic neoplasm, pyogenic abscess, tuberculoma, neurocysticercosis, resolving hematoma, tumefactive demyelination or radiation necrosis. [10],[11] However, in many cases, the clinical history can narrow the differential diagnosis. [11] At MRI, the toxoplasma lesions are multiple, commonly located in the deep central nuclei, posterior fossa or lobar at the gray-white matter junction, with prominent associated mass effect and edema and typically show intense rim enhancement after gadolinium administration. [4],[12] As in the present case, a cerebral toxoplasma abscess may have the same appearance as a pyogenic abscess on contrast-enhanced MRI. The toxoplasma lesions are hyperintense on T2- and hypointense on T1-weighted sequences. [11],[12] However, unlike water diffusion in the center of a pyogenic abscess, water diffusion is not restricted in the center of the toxoplasma abscess. [11],[12] Spectroscopy is characterized by a predominant lipid peak. [13] Presumptive diagnosis is considered in patients with <200 CD4+ T-lymphocyte cells/mL, anti-Toxoplasma IgG antibody in the serum, consistent clinical features, characteristic neuroimaging studies and response to empirical anti-Toxoplasma therapy. However, the definitive diagnosis can be made once there is direct demonstration of the tachyzoite form of the parasite in brain tissue. [14],[15],[16] As in the present case, rarely, the Mantoux test can be strongly positive even when the skin test for toxoplasmosis is negative. [17] The treatment of a case of cerebral toxoplasmosis includes pyrimethamin 50-100 mg/day and sulfadiazine 4 g/day. If the patient is allergic to sulfa drugs, he can alternatively be put on clindamycin 600 mg qid. [18]{Figure 1}{Figure 2}


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