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Toxoplasma lymphadenitis caused by ingestion of raw blood and meat of deer in a 10-year-old boy

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Toxoplasma lymphadenitis caused by

ingestion of raw blood and meat of deer in a 10-year-old boy

Chun Soo Kima,*, Dong Seok Kim a, Hye Ra Jung b

aDepartment of Pediatrics, Keimyung University School of Medicine, Daegu, South Korea

bDepartment of Pathology, Keimyung University School of Medicine, Daegu, South Korea

Received Jan 22, 2018; received in revised form Feb 26, 2018; accepted May 18, 2018 Available online 26 May 2018

Toxoplasma gondii infection in humans usually develops through the ingestion of raw or undercooked meat from an infected animal.1The presence of T. gondii DNA has been recently reported in the blood and milk of livestock, which can thus be another potential source of infection through the oral route.2

A 10-year-old boy presented with a 2-week history of unilateral cervical mass. Physical examination revealed an enlarged lymph node in the left posterior neck, measuring 3 cm in diameter, which was nontender, freely mobile, and firm. His past history showed that he sometimes drank raw blood (three times, total amount of 180 mL) and ate raw meat once (2 3 cm in size, three pieces) of the farm deer (Cervus nippon) for 2 weeks, about a month before the development of the mass on his neck. Ultrasound exami- nation revealed a lymph node measuring 3 1 cm in size at the posterior cervical area. A chemiluminescent immuno- assay (Access Toxo IgM II and IgG, Beckman Coulter Inc., USA) was performed for a serologic diagnosis of toxoplasma infection,3which revealed elevated antibody titers of 2.0 IU/mL for IgM (normal,<0.5 IU/mL), and >300 IU/mL for

IgG (normal,<2.0 IU/mL). Subsequently, an excisional bi- opsy of the neck mass was performed. Gross finding of the resected lymph node was unremarkable. Microscopic ex- aminations of the specimens showed characteristic findings suggestive of toxoplasma lymphadenitis (Fig. 1A and B), and protozoa were identified by immunohistochemical stains using primary polyclonal anti-T. gondii antibody (rabbit) (1:50, Cell Marque, USA) (Fig. 1C).4After the excision, he remained free of any cervical masses.

Although there is still a lack of data from Korea, ac- cording to a report from China, the seroprevalence of T.

gondii infection in domestic sika deer (C. nippon) has been found to be 13.5%.5Therefore, in the present case, both T.

gondii tachyzoites in the blood of the deer and tissue cysts in the venison were considered to be the source of infec- tion,2,6 this type of infection route in childhood has not been previously reported. In this case, the boy had eaten raw blood and meat of the farm deer due to inducement of his father who had a belief about its special nutritional value. An unreasonable custom for preservation of health can become an unexpected route of toxoplasma infection.

* Corresponding author. Department of Pediatrics, Keimyung University School of Medicine, 56 Dalseong-ro, Jung-gu, Daegu 41931, South Korea. Fax:þ82 53 250 7783.

E-mail address:[email protected](C.S. Kim).

https://doi.org/10.1016/j.pedneo.2018.05.008

1875-9572/Copyrightª 2018, Taiwan Pediatric Association. Published by Elsevier Taiwan LLC. This is an open access article under the CC BY- NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

Available online atwww.sciencedirect.com

ScienceDirect

j o u r n a l h o m e p a g e :h t t p : / / w w w . p e d i a t r - n e o n a t o l . c o m Pediatrics and Neonatology (2019) 60, 112e113

Downloaded for Anonymous User (n/a) at Keimyung University Dongsan Hospital from ClinicalKey.com by Elsevier on February 25, 2019.

For personal use only. No other uses without permission. Copyright ©2019. Elsevier Inc. All rights reserved.

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Conflict of interest

The authors have no conflicts of interest to declare.

Acknowledgements

This study was supported by the research promoting grant from the Institute for Medical Science of Keimyung Uni- versity in 2008.

References

1. Hill D, Dubey JP. Toxoplasma gondii: transmission, diagnosis and prevention. Clin Microbiol Infect 2002;8:634e40.

2. Mancianti F, Nardoni S, D’Ascenzi C, Pedonese F, Mugnaini L, Franco F, et al. Seroprevalence, detection of DNA in blood and

milk, and genotyping of Toxoplasma gondii in a goat population in Italy. Biomed Res Int 2013;2013:905326.

3.Mosti M, Pinto B, Giromella A, Fabiani S, Cristofani R, Panichi M, et al. A 4-year evaluation of toxoplasmosis seroprevalence in the general population and in women of reproductive age in central Italy. Epidemiol Infect 2013;141:2192e5.

4.Casartelli-Alves L, Boechat VC, Macedo-Couto R, Ferreira LC, Nicolau JL, Neves LB, et al. Sensitivity and specificity of sero- logical tests, histopathology and immunohistochemistry for detection of Toxoplasma gondii infection in domestic chickens.

Vet Parasitol 2014;204:346e51.

5.Qin SY, Zhang XX, Cong W, Zhou DH, Wang JL, Yin MY, et al.

Seroprevalence and risk factors of Toxoplasma gondii infection in domestic sika deer (Cervus nippon) in northeastern China. Acta Trop 2014;140:184e7.

6.Dubey JP. Re-examination of resistance of Toxoplasma gondii tachyzoites and bradyzoites to pepsin and trypsin digestion.

Parasitology 1998;116:43e50.

Figure 1 Histopathogical findings. (A) The lymph node shows reactive follicular hyperplasia and clusters of epithelioid histiocytes scattered in the paracortex and germinal center (H&E, 100). (B) Details of microgranuloma: epithelioid cells have abundant eosin- ophilic cytoplasm (H&E, 400). (C) Two T. gondii tachyzoites are noted in the lymph node (immunohistochemical stains, 1000).

Toxoplasma lymphadenitis 113

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Figure 1 Histopathogical findings. (A) The lymph node shows reactive follicular hyperplasia and clusters of epithelioid histiocytes scattered in the paracortex and germinal center (H&amp;E,  100)

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