Case Reports in Infectious Diseases

Case Reports in Infectious Diseases / 2019 / Article

Case Report | Open Access

Volume 2019 |Article ID 4603130 |

Federico Meconi, Giulia Ciangola, Benedetta Mariotti, Raffaella Cerretti, Laura Cudillo, William Arcese, Alessandra Picardi, "Cerebellar Neurocysticercosis as Long-Term Complication of Allogeneic Haematopoietic Stem Cell Transplantation from Haploidentical Donor", Case Reports in Infectious Diseases, vol. 2019, Article ID 4603130, 4 pages, 2019.

Cerebellar Neurocysticercosis as Long-Term Complication of Allogeneic Haematopoietic Stem Cell Transplantation from Haploidentical Donor

Academic Editor: Peter Olumese
Received25 Jan 2019
Revised09 Jul 2019
Accepted06 Sep 2019
Published19 Sep 2019


Neurocysticercosis, an infection of the central nervous system with the larval stage of the cestode Taenia solium, is uncommon in developed countries. We report a case of allogeneic haematopoietic stem cell transplantation from a haploidentical donor complicated, in the long term, by T. solium infection of the central nervous system and successfully treated with empiric antiparasitic therapy with albendazole plus dexamethasone. Revised diagnostic criteria proposed by Del Brutto et al. were used for the definitive diagnosis of cerebellar neurocysticercosis.

1. Introduction

Cysticercosis is the most common parasitic disease of the central nervous system (CNS) in humans [1], caused by infection of Taenia solium, the larval stage of the tapeworm found in pigs. Human cysticercosis results from fecal-oral contamination with Taenia solium eggs from a human tapeworm carrier. People living in rural setting are at increased risk for exposure. Clinical manifestations are nonspecific and depend on locations, number, size of cysts, and host immune response to the cysticerci. In the CNS, it frequently involves the cerebral hemispheres and cortex and rarely involves ventricles and basal cisterns, subarachnoid space, and spine [2]. When the cysts coalesce to form a tree-like pattern it is known as racemose neurocysticercosis (NCC). Diagnosis of NCC is often difficult due to dangerous brain localization and lack of laboratory specific tests. Revised diagnostic criteria, proposed by Del Brutto et al. [3], as reported in Table 1, may be useful for the definitive diagnosis of NCC.

Categories of criteriaCriteria

Absolute(i) Histological demonstration of the parasite from biopsy of a brain or spinal cord lesion
(ii) Visualization of subretinal cysticercus
(iii) Conclusive demonstration of a scolex within a cystic lesion on neuroimaging studies

NeuroimagingMajor neuroimaging criteria
(i) Cystic lesions without a discernible scolex
(ii) Enhancing lesionsa
(iii) Multilobulated cystic lesions in the subarachnoid space
(iv) Typical parenchymal brain calcificationsa
Confirmative neuroimaging criteria
(i) Resolution of cystic lesions after cysticidal drug therapy
(ii) Spontaneous resolution of single small enhancing lesionsb
(iii) Migration of ventricular cysts documented on sequential neuroimaging studiesa
Minor neuroimaging criteria
(i) Obstructive hydrocephalus (symmetric or asymmetric) or abnormal enhancement of basal leptomeninges

Clinical/exposureMajor clinical/exposure
(i) Detection of specific anticysticercal antibodies or cysticercal antigens by well-standardized immunodiagnostic testsa
(ii) Cysticercosis outside the central nervous systema
(iii) Evidence of a household contact with T. solium infection
Minor clinical/exposure
(i) Clinical manifestations suggestive of neurocysticercosisa
(ii) Individuals coming from or living in an area where cysticercosis is endemica
Definitive diagnosis
(i) One absolute criterion
(ii) Two major neuroimaging criteria plus any clinical/exposure criteria
(iii) One major and one confirmative neuroimaging criteria plus any clinical/exposure criteria
(iv) One major neuroimaging criteria plus two clinical/exposure criteria (including at least one major clinical/exposure criterion) together with the exclusion of other pathologies producing similar neuroimaging findings
Probable diagnosis
(i) One major neuroimaging criteria plus any two clinical/exposure criteria
(ii) One minor neuroimaging criteria plus at least one major clinical/exposure criteria

aOperational definitions. Cystic lesions: rounded, well-defined lesions with liquid contents of signal similar to that of the CSF on CT or MRI; enhancing lesions: single or multiple, ring- or nodular-enhancing lesions of 10–20 mm in diameter, with or without surrounding edema, but not displacing midline structures; typical parenchymal brain calcifications: single or multiple, solid, and most usually <10 mm in diameter; migration of the ventricular cyst: demonstration of a different location of ventricular cystic lesions on sequential CTs or MRIs; well-standardized immunodiagnostic tests: so far, antibody detection by the enzyme-linked immunoelectrotransfer blot assay using lentil lectin-purified T. solium antigens, and detection of cysticercal antigens by monoclonal antibody-based ELISA; cysticercosis outside the central nervous system: demonstration of cysticerci from biopsy of subcutaneous nodules, X-ray films, or CT showing cigar-shaped calcifications in soft tissues, or visualization of the parasite in the anterior chamber of the eye; suggestive clinical manifestations: mainly seizures (often starting in individuals aged 20–49 years; the diagnosis of seizures in this context is not excluded if patients are outside of the typical age range), but other manifestations include chronic headaches, focal neurologic deficits, intracranial hypertension, and cognitive decline; cysticercosis-endemic area: a place where active transmission is documented. bThe use of corticosteroids makes this criterion invalid.

Here in, we report a case of a cerebellar racemose NCC as a long-term complication of allogeneic haematopoietic stem cell transplantation (HSCT) from a haploidentical donor.

2. Case Presentation

A 64-year-old female underwent haploidentical allogeneic HSCT for diagnosis of acute myeloid leukemia secondary to myelodysplastic syndrome in September 2016. A haploidentical son, 41 years old, 0 Rh positive, EBV, CMV, and toxoplasma IgG positive, was selected as the donor because of the lack of a well-matched unrelated stem cell donor according to our transplant policy [4, 5].

The Valencia schedule, consisting of a combination of reduced dose of thiotepa, Busilvex, and fludarabine, was used [6] as a conditioning regimen, while the association of cyclosporine (0.75 mg/Kg/12 h continuous infusion from day –7, increased from day –1 to 1.5 mg/Kg/12 h continuous infusion), a short course of methotrexate (15 mg/mq on day 1 and 10 mg/mq on day 3–6 and 11), rabbit anti-thymocyte globulin (ATG) (5 mg/Kg/die from day –4 to day –1), basiliximab (20 mg on day 0 and day +4), and mycophenolic acid (15 mg/Kg twice daily) was administered as GVHD prophylaxis.

On day +100 after transplant, she developed acute gastrointestinal (GI) tract (stage 1, grade 2) GVHD successfully treated with steroids. Transplant-related complications due to the consequent use of a high-dose steroid for long time for GVHD included multiple episodes of reactivation of cytomegalovirus responded to antiviral therapy, sarcopenia, and fracture of the head of the femur surgically resolved.

On day +320 after transplant, the patient presented with nausea, vomiting, nystagmus, diplopia, and severe cutaneous purpura. A CT scan of the head showed a right multicystic cerebellar mass with perilesional edema compressing the fourth ventricle, also confirmed by brain MRI. As the lesions were not previously reported, we ruled out congenital abnormalities such as cavernous malformations. Since other differential diagnosis, including infectious (tuberculotic, echinococcal, and toxoplasmotic cysts) and neoplastic diseases, required a histological assessment, we proceeded to a surgical excision of one of the neuroradiological lesions.

An attempted biopsy of the cystic lesions, through suboccipital craniotomy, failed due to moderate bleeding during surgery. Histologic findings showed normal cerebellar tissue with polymorphonuclear leukocytes. Although the available specimen was not sufficient for all diagnostic tests, no neoplastic cells or fungal hyphae were seen. The fundus oculi assessment did not show cystis. Moreover, the quantiferon and TB skin test (or PPD test) were negative. Although prompt empiric antibiotic combination of meropenem and clindamycin was started, clinical and neuroradiological response was not achieved. High-dose intravenous trimethoprim-sulfamethoxazole for a suspicious cerebral toxoplasmosis, due to donor and patient IgG positivity before HSCT, was given after 20 days of antibiotic therapy. After two weeks of this therapy, continued clinical symptoms and MRI of the brain showed worsening of multicystic lesions with perifocal edema and initial cerebellar herniation. The patient also developed an intention tremor, bilateral hypoacusia, and severe haematological toxicity. In absence of clinical and radiological improvement and taking into account the patient’s history of living in countryside, we applied the revised diagnostic criteria for Taenia solium infection and discovered that our patient presented a definitive diagnosis of NCC due to the neuroimaging presence of cystic lesions without a discernible scolex and enhancing lesion plus previous household contact with T. solium and neurological clinical manifestations of NCC. Moreover, in this case we documented the resolution of cystic lesions after cysticidal drug therapy (Figure 1), as confirmative criterion.

However, no cystic lesions were found in muscles, and the IgG Elisa test in blood and 3 consecutive stool samples were negative for T. Solium. The patient started empiric antiparasitic treatment with albendazole (400 mg PO BID) plus intravenous administration of dexamethasone (4 mg/day). Lumbar puncture was not performed due to high risk of hernia wedging and MRI signs of hydrocephalus. After 14 days, brain MRI control showed disappearance of some of the cystic lesions in the right cerebellar hemisphere and the reduction in size of some others. Patient was released from the hospital with no neurological symptoms, continuing albendazole therapy for four months.

3. Discussion

Despite the fact that NCC is the most common parasitic infection of the CNS and one of the main causes of acquired epilepsy worldwide [7], the diagnosis process is still difficult and sometimes it is feasible only through the exclusion of similar diseases. Clinical symptoms are very heterogeneous, depending on the location of cystic lesions in the CNS. Acquired seizures are the most common symptoms but also chronic headaches, focal neurological deficits, intracranial hypertension, and cognitive decline are described as frequent. Furthermore, it is not always possible to biopsy these lesions to obtain histological confirmation of the parasite colonization due to localization in the CSN. According to Del Brutto et al. revised diagnostic criteria, in the case reported here, the definitive diagnosis was made thanks to the association of neuroimaging with clinical features that together may be considered highly sensitive and specific of this rare disease as well described by Bustos et al. [8].

In developed countries, CNS infection by uncommon parasites is very rare, also in patients with severe immunosuppression due to chemotherapy, HSCT, and HIV. However, emerging germs must be reconsidered due to the migration flux from other countries where they are still endogenous.

Since immunosuppression is deeper in the haematopoietic stem cell transplants than organ transplants, patients’ anamnestic history should include questions about previous contact with parasites. Moreover, specific hygienic rules should be recommended in discharged patients. Finally, living in rural areas or contact with swines must be strongly advised against after the HSCT procedure.

To the best of our knowledge, there is no evidence that previous exposure to T. Solium is an absolute contraindication to HSCT. Furthermore, it is still matter of debate if these patients could benefit of a prophylaxis or a pre-emptive antiparasitic therapy as it is now recommended for P. jirovecii, cytomegalovirus, and herpes viruses.

Barra Valencia et al. have reported one case of CNS cystercosis infection after transplant for solid organs [9]; only two reports of NCC have been reported as short-term complication (3–4 months) after allogeneic haematopoietic stem cell transplant (HSCT) [10, 11]. This case report represents a rare cerebellar racemose cysticercosis localization of T. Solium as long-term complication of haploidentical HSCT and underlines the adjunctive risk of the environmental factors, beyond the slow immunological recovery, on the transplant outcome of this subset of patients.

This case report highlights a rare and dangerous case of an opportunistic infection, presenting as a late complication after haploidentical allogeneic transplant and the importance of collecting complete patient’s history before transplant in order to identify all individual risk factors. Reestablishment of immunocompetence requires at least several months, and some patients continue to demonstrate immune deficits for several years after HSCT (in general NK cells are the first lymphocyte subset to recover, followed by CD8+ T cells, B cells, and ultimately CD4+ T cells). CD4+ count is probably the most predictive marker of the restoration of immune competence, and several studies have demonstrated that CD4+ recovery is associated with diminished infectious risk and improved transplant outcomes. Nowadays, there is a clinical need for specific environmental guidelines for this cohort of patients to avoid behaviors at high infectious risk. Safe living after HSCT includes preventing infections primarily transmitted by direct contact (hand hygiene), infections primarily transmitted through respiratory exposures (contact with persons with respiratory illnesses or plants, soil, or their aerosols), and pet-transmitted zoonotic infections. Additional food safety practices appropriate for HSCT recipients include avoiding undercooked meat and using separated cutting boards [9]. Moreover, in this setting, the possibility and timing for resuming previous habits in life should be better defined. Finally, the recent introduction of chimeric antigen receptor T cells [10] infusions represents a very promising tool to improve the immunological recovery after haploidentical HSCT and could minimize the development of CNS infections too.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.


  1. A. C. White Jr., “Neurocysticercosis: updates on epidemiology, pathogenesis, diagnosis, and management,” Annual Review of Medicine, vol. 51, no. 1, pp. 187–206, 2000. View at: Publisher Site | Google Scholar
  2. R. R. Mahale, A. Mehta, and S. Rangasetty, “Extraparenchymal (racemose) neurocysticercosis and its multitude manifestations: a comprehensive review,” Journal of Clinical Neurology, vol. 11, no. 3, p. 203, 2015. View at: Publisher Site | Google Scholar
  3. O. H. Del Brutto, T. E. Nash, A. C. White et al., “Revised diagnostic criteria for neurocysticercosis,” Journal of the Neurological Sciences, vol. 372, pp. 202–210, 2017. View at: Publisher Site | Google Scholar
  4. W. Arcese, I. Mangione, and A. Picardi, “Algorithm for donor selection in 2011,” Current Opinion in Hematology, vol. 18, no. 6, pp. 401–407, 2011. View at: Publisher Site | Google Scholar
  5. A. Picardi, W. Arcese, S. Pollichieni et al., “The Rome transplant network model compared to the Italian bone marrow donor registry activity for unrelated donor search process and transplant efficiency for hematologic malignancy,” Transfusion, vol. 57, no. 7, pp. 1734–1743, 2017. View at: Publisher Site | Google Scholar
  6. J. Sanz, C. Martín, J. C. H. Boluda et al., “Single-unit umbilical cord blood transplantation from unrelated donors in patients with hematological malignancy using busulfan, thiotepa, fludarabine and ATG as myeloablative conditioning regimen,” Bone Marrow Transplantation, vol. 47, no. 10, pp. 1287–1293, 2012. View at: Publisher Site | Google Scholar
  7. H. H. Garcia, “Neurocysticercosis,” Neurologic Clinics, vol. 36, no. 4, pp. 851–864, 2018. View at: Publisher Site | Google Scholar
  8. J. A. Bustos, H. H. García, and O. H. Del Brutto, “Reliability of diagnostic criteria for neurocysticercosis for patients with ventricular cystic lesions or granulomas: a systematic review,” The American Journal of Tropical Medicine and Hygiene, vol. 97, no. 3, pp. 653–657, 2017. View at: Publisher Site | Google Scholar
  9. V. Barra Valencia, A. Moreno Elola-Olaso, Y. Fundora Suárez et al., “Second case of neurocysticercosis in a patient with liver transplantation (first case in Spain): a case report,” Transplantation Proceedings, vol. 39, no. 7, pp. 2454–2457, 2007. View at: Publisher Site | Google Scholar
  10. S. Purvey, K. Lu, S. K. Mukkamalla et al., “Conservative management of neurocysticercosis in a patient with hematopoietic stem cell transplantation: a case report and review,” Transplant Infectious Disease, vol. 17, no. 3, pp. 456–462, 2015. View at: Publisher Site | Google Scholar
  11. L. Illade, B. Molina Angulo, I. Solís, M. Á. Diaz, and M. Gonzalez-Vicent, “Neurocysticercosis: an unusual seizure etiology in a hematopoietic stem cell transplanted patient,” Pediatric Hematology and Oncology, vol. 35, no. 1, pp. 20–22, 2018. View at: Publisher Site | Google Scholar

Copyright © 2019 Federico Meconi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles