Next Article in Journal
A Comparative Study on Distancing, Mask and Vaccine Adoption Rates from Global Twitter Trends
Next Article in Special Issue
Prediction of Cardiovascular Risk Using Nonalcoholic Fatty Liver Disease Scoring Systems
Previous Article in Journal
Predicting Hospital Overall Quality Star Ratings in the USA
Previous Article in Special Issue
Communication on Safe Caregiving between Community Nurse Case Managers and Family Caregivers
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Case Report

Toxoplasmic Lymphadenitis Presenting as a Tiny Neck Tumor

1
Department of Otolaryngology & Head and Neck Surgery, Chang Gung Memorial Hospital, Linkou 333, Taiwan
2
School of Medicine, Chang Gung University, Taoyuan 333, Taiwan
3
Department of Pathology, Keelung Chang Gung Memorial Hospital, Keelung 204, Taiwan
4
Department of Otolaryngology & Head and Neck Surgery, Chang Gung Memorial Hospital, Keelung 204, Taiwan
*
Author to whom correspondence should be addressed.
Healthcare 2021, 9(5), 487; https://doi.org/10.3390/healthcare9050487
Submission received: 31 March 2021 / Revised: 17 April 2021 / Accepted: 19 April 2021 / Published: 21 April 2021
(This article belongs to the Special Issue Family Medicine: Opportunities and Challenges for Primary Healthcare)

Abstract

:
(1) Background: Toxoplasmic lymphadenitis (TL), caused by the protozoan Toxoplasma gondii, is a worldwide zoonosis. We report a case of TL in the head and neck region diagnosed using ultrasound (US)-guided fine needle aspiration cytology (FNAC), serological tests, and pathological findings. (2) Case Presentation: A 51-year-old female with a chief complaint of a left posterior neck mass that had been growing for approximately 2 weeks. TL was confirmed by histopathological examinations and serological tests. US-guided FNAC and en bloc resection of the lymph node were performed. The diagnosis was confirmed as TL in the neck. (3) Conclusions: We suggest that US-guided FNAC should be considered as the first-line test for assessing a tiny mass before a definitive treatment is chosen.

1. Introduction

The prevalence of toxoplasmosis is increasing globally. In Taiwan, the overall seroprevalence of Toxoplasmic gondii (T. gondii) infection is 9.3% in the major regions [1]. Toxoplasmic lymphadenitis (TL) caused by T. gondii primarily involves the neck and occipital areas. Other frequent sites include the axillary, submental, inguinal, and supraclavicular lymph nodes, and ocular and cerebral areas [2]. Here, we describe a patient who presented with a painless, enlarged mass in the left posterior neck. We used ultrasound (US)-guided fine needle aspiration cytology (FNAC) and surgical intervention to approach the mass lesion, and confirm the diagnosis of TL.

2. Case Presentation

A 51-year-old female came to our department with a chief complaint of a left posterior mass that had been growing for approximately 2 weeks. The patient had no fever, night sweats, weight loss, traumatic episode, surgical history, or painful sensations, and no specific medical disease or systemic disorder. She had owned a dog for 3 years. A physical examination revealed a well-defined mass in the left posterior triangle of her neck. Laboratory findings showed a normal C-reactive protein level (4.80 mg/L; normal: <5 mg/L) without leukocytosis (9500/µL; normal: 3900–10,600/µL). To differentiate this mass lesion, we arranged US-guided FNAC. Target US revealed an ovoid hypovascular hypoechoic lymph node with a short axis of about 0.6 cm and preserved fatty hilum. (Figure 1A). FNAC was performed at the site using a 21-gauge needle (Figure 1B). The cytological findings showed a mixed lymphocytic population alone. An en bloc resection of the lymph node was conducted (Figure 2A,B). The specimen consisted of a grayish and soft mass measuring about 1.0 × 0.7 × 0.6 cm 3. The section of the specimen displayed a preserved nodal architecture with reactive follicular hyperplasia and the presence of small clusters of epithelioid histiocytes at the periphery of germinal centers in the affected lymph node (Figure 3). After the pathological report was available, we further completed the relevant serological tests, which revealed elevated levels of Toxoplasma IgG (513.70 IU/mL; normal: <1.6 mg/L) and Toxoplasma IgM (1.46 index; normal: <0.5 index). TL of the head and neck region was confirmed.
Based on the histopathological report and serological results, an infection specialist prescribed pyrimethamine (25 mg/tab) to treat the T. gondii infection. The postoperative surgical wound healed well. The patient’s Toxoplasma IgG and IgM levels returned to the normal range at the completion of the treatment course.

3. Discussion

TL is a worldwide zoonosis caused by the protozoan parasite T. gondii [3,4]. We report a patient with TL of the head and neck region diagnosed using FNAC, serological tests, and histopathological findings.
Toxoplasma gondii is estimated to infect about 50% of the population in the United States [5] and Europe [6]. The three transmission routes include food origin (consumption of meat infected with Toxoplasma cysts), animal-to-human infection (intake of oocysts shed in the feces of infected cats), and mother-to-fetus infection (congenital infection during pregnancy) [1]. Additionally, T. gondii can be transmitted through blood transfusions or organs transplanted from infected donors. A nationwide study in Taiwan found that the consumption of raw shellfish and raising a cat were independent risk factors for infection of T. gondii infection [1]. TL is most commonly seen in older children and young adults and occurs more frequently in females than in males [7]. The seasonal prevalence of TL is highest in the winter months. A retrospective study performed at a Pakistani medical institute found that the most common occupations of people with TL were students (48.8%), soldiers (18.6%), housewives (11.6%), teachers (9.3%), and drivers (6.9%) [8].
The majority of T. gondii infections are asymptomatic and self-limiting in immunocompetent hosts; however, symptomatic disease can occur in immunocompromised individuals [4,5]. The enlargement of single or multiple superficial lymph nodes is the most common sign of acquired toxoplasmosis in humans [7,9]. The most common site of TL is the neck (69.7%) followed by the axillary (6.9%), submental (4.6%), inguinal (4.6%), and supraclavicular (2.3%) lymph nodes, and other areas (11.6%) [8]. In the neck, the posterior area is most commonly affected [5]. TL is usually painless and non-suppurative. Other symptoms may include fatigue, general weakness without a fever or weight loss, diarrhea, increasing tiredness, and myalgias [10]. Toxoplasma infections usually occur in nasopharyngeal lymphoid tissue, which is consistent with cervical lymph node involvement without a sore throat [7]. However, if a fever occurs, infectious mononucleosis should be considered and a blood smear examined for lymphocytosis with atypical lymphocytes. Further, prolonged and persistent enlargement of the lymph node(s) for months or years may warrant clinical suspicion of a malignant lymphoma [7]. Ahmad et al. found that in the final pathological diagnosis as TL, the differential diagnosis clinically included tuberculosis lymphadenitis (55.8%), Hodgkin’s disease (16.2%), malignant lymphoma (11.6%), chronic lymphadenitis (4.6%), infectious mononucleosis (2.3%), reactive changes (2.3%), and no specific diagnosis (6.9%) [8].
Several imaging tools have been shown to be useful for the diagnosis of TL, including US-guided FNA, CT, and magnetic resonance imaging (MRI). US allows the visualization of homogeneous, well-defined enlarged lymph nodes. Kojima et al. found FNAC to be a simple, safe, economical, and quick assessment procedure for TL [11]. Conversely, Cho et al. recommended core needle biopsy (CNB) as the first-line investigation for lymphadenopathy [12].
The infected lymph node was enlarged; however, there was nothing distinctive about the macroscopic appearance [7]. Lymphoid hyperplasia accounted for the enlargement [13]. The follicles were large and irregularly shaped with active germinal centers. Pale-staining histiocytes with an eosinophilic cytoplasm were scattered around the pulp of the lymph node and invaded the follicles. These cells were similar to the epithelioid cells of tuberculosis; however, caseation was absent. Moreover, the cells were less sharp and smaller than the collections of cells seen in sarcoidosis. Histiocytic clusters are characteristic of TL [7]. Weiss et al. noted that a pathological findings in lymph nodes with TL often contain the characteristic triad of reactive follicular hyperplasia, irregular clusters of epithelioid histiocytes (blurring the germinal centers), and focal trabecular and subcapsular sinuses distended by monocytoid B cells [5].
TL can be confirmed by serological tests in the majority of patients and is a primary method for diagnosis [4]. Increasing titers of cytoplasm-modifying antibodies can be considered an active infection [7]. Contini et al. noted that elevated IgM antibody titers were indicative of an acute infection [4]. In fact, the positive serological findings have shown to be sufficient for the diagnosis of TL [7]. PCR has not been used to definitively diagnose TL, although, in some reports, it was applied to biopsy material.
Pyrimethamine and sulfadiazine remain the first-line treatments for toxoplasmosis.
Trimethoprim–sulphamethoxazole is an alternative medication for patients who cannot tolerate pyrimethamine and sulfadiazine [2].

4. Conclusions

We detected TL in the head and neck region of a patient presenting with an enlarged and painless mass. US with FNA should be considered as the first-line test for assessing a mass before a definitive treatment is chosen. Although the diagnosis of TL in the head and neck region is challenging, the combined use of FNAC, biopsy, and serological tests will help clinicians achieve an accurate result.

Author Contributions

Conceptualization, S.-L.C.; J.-R.C.; S.-W.Y.; methodology, S.-L.C.; S.-W.Y.; validation, S.-L.C.; S.-W.Y.; data curation, S.-L.C.; J.-R.C.; S.-W.Y.; writing—original draft preparation, S.-L.C.; writing—review and editing, S.-L.C.; S.-W.Y.; visualization, S.-L.C.; J.-R.C.; S.-W.Y.; supervision, S.-L.C.; J.-R.C.; S.-W.Y.; project administration, S.-L.C.; J.-R.C.; S.-W.Y. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The publication of this case report was approved by the Institutional Review Board of Chang Gung Memorial Hospital (IRB No. 201901220B0).

Informed Consent Statement

Informed consent was obtained from all subjected involved in the study.

Data Availability Statement

All data generated or analyzed during this study are included in this published article.

Acknowledgments

The authors thank all of the members of Department of Otolaryngology—Head and Neck Surgery, Chang Gung Memorial Hospital, Keelung, for their invaluable help. The English in this document has been checked by at least two professional editors, both native speakers of English. For a certificate, please see: http://www.textcheck.com/certificate/i7dZI2 (accessed on 30 September 2019).

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

TL = toxoplasmic lymphadenitis; FNAC = fine needle aspiration cytology; US = ultrasound; CT = computed tomography; PCR= polymerase chain reaction.

References

  1. Chiang, T.Y.; Kuo, M.C.; Chen, C.H.; Yang, J.Y.; Kao, C.F.; Ji, D.D.; Fang, C.T. Risk factors for acute Toxoplasma gondii diseases in Taiwan: A population-based case-control study. PLoS ONE 2014, 9, e90880. [Google Scholar] [CrossRef] [PubMed]
  2. Rajapakse, S.; Chrishan Shivanthan, M.; Samaranayake, N.; Rodrigo, C.; Deepika Fernando, S. Antibiotics for human toxoplasmosis: A systematic review of randomized trials. Pathog. Glob. Health 2013, 107, 162–169. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Aisner, S.C.; Aisner, J.; Moravec, C.; Arnett, E.N. Acquired toxoplasmic lymphadenitis with demonstration of the cyst form. Am. J. Clin. Pathol. 1983, 79, 125–127. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Contini, C.; Giuliodori, M.; Cultrera, R.; Seraceni, S. Detection of clinical-stage specific molecular Toxoplasma gondii gene patterns in patients with toxoplasmic lymphadenitis. J. Med. Microbiol. 2006, 55, 771–774. [Google Scholar] [CrossRef] [PubMed]
  5. Weiss, L.M.; Chen, Y.Y.; Berry, G.J.; Strickler, J.G.; Dorfman, R.F.; Warnke, R.A. Infrequent detection of Toxoplasma gondii genome in toxoplasmic lymphadenitis: A polymerase chain reaction study. Hum. Pathol. 1992, 23, 154–158. [Google Scholar] [CrossRef]
  6. Kikuchi, M.; Yoshizumi, T.; Nakamura, H. Necrotizing lymphadenitis: Possible acute toxoplasmic infection. Virchows Arch. A Pathol. Anat. Histol. 1977, 376, 247–253. [Google Scholar] [CrossRef] [PubMed]
  7. Stansfeld, A.G. The histological diagnosis of toxoplasmic lymphadenitis. J. Clin. Pathol. 1961, 14, 565–573. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Ahmad, M.; Iqbal, J.; Mansoor, A.; Khan, A.H. Toxoplasmic lymphadenitis—A clinicopathological study. J. Pak. Med. Assoc. 1991, 41, 303–305. [Google Scholar] [PubMed]
  9. McCabe, R.E.; Brooks, R.G.; Dorfman, R.F.; Remington, J.S. Clinical spectrum in 107 cases of toxoplasmic lymphadenopathy. Rev. Infect. Dis. 1987, 9, 754–774. [Google Scholar] [CrossRef] [PubMed]
  10. Cohen, C.; Trapuckd, S. Toxoplasma cyst with toxoplasmic lymphadenitis. Hum. Pathol. 1984, 15, 396–397. [Google Scholar] [CrossRef]
  11. Kojima, M.; Shimizu, K.; Kaba, S.; Itoh, H. Imprint cytology specimen of toxoplasmic lymphadenitis containing numerous large clusters of monocytoid B-cells: Two case reports. Diagn. Cytopathol. 2008, 36, 196–198. [Google Scholar] [CrossRef] [PubMed]
  12. Cho, W.; Kim, M.K.; Sim, J.S. Ultrasound-guided core needle biopsy of cervical lymph nodes in the diagnosis of toxoplasmosis. J. Clin. Ultrasound 2017, 45, 192–196. [Google Scholar] [CrossRef] [PubMed]
  13. Ito, M.; Hara, K.; Saga, S.; Asai, J.; Iijima, S. Two cases of acquired toxoplasmic lymphadenitis. Light and electron microscopic and immunohistochemical studies. Acta Pathol. Jpn. 1988, 38, 1565–1573. [Google Scholar] [CrossRef] [PubMed]
Figure 1. (A) Targeted ultrasound revealed an ovoid hypovascular hypoechoic mass with a short axis of about 0.6 cm and preserved. (B) Fine needle aspiration cytology was performed using a 21-gauge needle.
Figure 1. (A) Targeted ultrasound revealed an ovoid hypovascular hypoechoic mass with a short axis of about 0.6 cm and preserved. (B) Fine needle aspiration cytology was performed using a 21-gauge needle.
Healthcare 09 00487 g001
Figure 2. (A) A well-defined and soft mass was noted in the left posterior neck. No erythematous change or local heat over the skin was observed. (M: mass). (B) The incision was made above the mass. The left neck mass (arrowhead) was explored and en bloc resection was conducted.
Figure 2. (A) A well-defined and soft mass was noted in the left posterior neck. No erythematous change or local heat over the skin was observed. (M: mass). (B) The incision was made above the mass. The left neck mass (arrowhead) was explored and en bloc resection was conducted.
Healthcare 09 00487 g002
Figure 3. Microscopic examination revealed reactive follicular hyperplasia (arrowhead) and the presence of small clusters of epithelioid histiocytes (arrow) in the affected lymph node (original magnification ×40).
Figure 3. Microscopic examination revealed reactive follicular hyperplasia (arrowhead) and the presence of small clusters of epithelioid histiocytes (arrow) in the affected lymph node (original magnification ×40).
Healthcare 09 00487 g003
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Chen, S.-L.; Chen, J.-R.; Yang, S.-W. Toxoplasmic Lymphadenitis Presenting as a Tiny Neck Tumor. Healthcare 2021, 9, 487. https://doi.org/10.3390/healthcare9050487

AMA Style

Chen S-L, Chen J-R, Yang S-W. Toxoplasmic Lymphadenitis Presenting as a Tiny Neck Tumor. Healthcare. 2021; 9(5):487. https://doi.org/10.3390/healthcare9050487

Chicago/Turabian Style

Chen, Shih-Lung, Jim-Ray Chen, and Shih-Wei Yang. 2021. "Toxoplasmic Lymphadenitis Presenting as a Tiny Neck Tumor" Healthcare 9, no. 5: 487. https://doi.org/10.3390/healthcare9050487

APA Style

Chen, S. -L., Chen, J. -R., & Yang, S. -W. (2021). Toxoplasmic Lymphadenitis Presenting as a Tiny Neck Tumor. Healthcare, 9(5), 487. https://doi.org/10.3390/healthcare9050487

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop