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CYTOJOURNAL QUIZ CASE
CytoJournal 2019,  16:15

A rare case of malignant metastatic tumor diagnosed on fine-needle aspiration of cervical lymph node


Department of Pathology, Postgraduate Institute of Medical Education and Research, Dr. RML Hospital, New Delhi, India

Date of Submission07-Jul-2018
Date of Acceptance28-Nov-2018
Date of Web Publication25-Jul-2019

Correspondence Address:
Arvind Ahuja
Department of Pathology, Postgraduate Institute of Medical Education and Research, Dr. RML Hospital, New Delhi
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/cytojournal.cytojournal_26_18

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How to cite this article:
Ahuja A, Kumari S. A rare case of malignant metastatic tumor diagnosed on fine-needle aspiration of cervical lymph node. CytoJournal 2019;16:15

How to cite this URL:
Ahuja A, Kumari S. A rare case of malignant metastatic tumor diagnosed on fine-needle aspiration of cervical lymph node. CytoJournal [serial online] 2019 [cited 2019 Oct 19];16:15. Available from: http://www.cytojournal.com/text.asp?2019/16/1/15/263420

Editorial/Peer Review Statement
To ensure the integrity and highest quality of CytoJournal publications, the review process of this manuscript was conducted under a double-blind model (authors are blinded for reviewers and vice versa) through automatic online system.


A 57-year-old female came to ear, nose, throat outpatient department with painless right-side cervical swelling for 1½ years. On examination, she had an enlarged right cervical lymph node in the middle part of the neck, measuring approximately 3 cm in diameter. It was firm, mobile, and nontender. Fine-needle aspiration cytology (FNAC) was performed from the cervical lymph node to establish the diagnosis [Figure 1].
Figure 1: Fine-needle aspiration cytology. (a and b) Cellular smears showing loose cohesive clusters of tumor cells with acinar follicular pattern in a background of reactive lymphoid cells (a: MGG, ×100; b: PAP, ×100). (c) High power showing round-to-oval nucleus with moderate anisonucleosis and bizarre cell (MGG, ×400). (d) Tumor cell showing fine nuclear chromatin and moderate-to-abundant fragile cytoplasm and lymphocyte sprinkling (PAP, ×400)

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 » Question Top


What is your Interpretation?

  1. Reactive lymphoid proliferation
  2. Non-caseating granuloma
  3. Metastatic paraganglioma
  4. Metastatic follicular carcinoma.



 » Answer Top


The correct cytopathology interpretation is: C. Metastatic paraganglioma

On microscopic examination, the smears were cellular and showed many loose cohesive clusters and dispersed tumor cells in a background of abundant reactive lymphoid cells and hemorrhage [Figure 1]a and [Figure 1]b. The tumor cells were arranged in focal acinar or follicular pattern with a round-to-oval nucleus, moderate anisonucleosis, fine nuclear chromatin, and moderate-to-abundant fragile cytoplasm with the focal presence of fine granules. Few bizarre and binucleated tumor cells were also noted [Figure 1]c and [Figure 1]d. On the basis of characteristic cytological features, a diagnosis of metastatic neuroendocrine tumor/paraganglioma was suggested.

In view of the cytological diagnosis, the patient was further evaluated by ultrasonography and contrast-enhanced computerized tomography (CECT) of the neck. CECT revealed, in addition, a lobulated, ill-marginated enhancing space-occupying mass in the right carotid bifurcation. It was in close proximity to right common carotid artery beginning at the level of carotid bifurcation. It measured approximately 3.4 cm × 3.2 cm × 3.2 cm [Figure 2]. On color Doppler evaluation, the lesion was observed to lie between the internal and external carotid arteries. She underwent surgery, and resection of the tumor with neck dissection was performed, which was reported as malignant carotid body paraganglioma on histopathology.
Figure 2: Contrast-enhanced computerized tomography showing a lobulated, ill-marginated enhancing space occupying lesion in the right carotid bifurcation

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 » Additional Quiz Questions Top


Q1: Which is the most common site of paraganglioma?

  1. Carotid body
  2. Adrenal gland
  3. Mediastinum
  4. Organ of Zuckerkandl.


Q2: Following immunohistochemistry (IHC), which IHC marker is not expressed in paraganglioma?

  1. S-100
  2. Pan-cytokeratin
  3. Synaptophysin
  4. Neuron-specific enolase.


Q3: Which of the following is the diagnostic feature of malignant paraganglioma?

  1. Pleomorphism
  2. Mitosis
  3. Metastases
  4. All the above.



 » Answers to the Additional Questions Top


Q1: b; Q2: b; and Q3: c

Q1: (b) Adrenal gland accounts for 90% of paraganglioma, which is also known as pheochromocytoma at this site. Extraadrenal paraganglioma accounts for the rest 10%–15% cases. The most common extraadrenal site is the carotid body and the organ of Zuckerkandl[1]

Q2: (b) The chief cells of paraganglioma show positive immunostaining with chromogranin, synaptophysin, and neuron-specific enolase, whereas S-100 and glial fibrillary acidic proteins are positive in stellate or dendritic sustentacular cells.[1] Pan-cytokeratin is negative in both the cells

Q3: (c) Malignant paraganglioma is diagnosed only when it metastasizes to the regional lymph node or distant organs such as the liver, bone, or lungs.[1] There are no accepted cytological or histopathological criteria for the diagnosis of malignancy in paraganglioma. Multicentric paraganglioma must be distinguished from the true metastases.


 » Brief Review of the Topic Top


Paraganglia are collections of specialized neural crest cells arising in association with the autonomic ganglia. Tumors arising from these cells are called paragangliomas, and their names depend on their site.[2],[3] Carotid body paraganglioma is the most common extraadrenal paraganglioma in the head-and-neck region.[2],[3] It is situated in the adventitia of the posteromedial aspect of the common carotid artery bifurcation. The usual clinical presentation is that of a painless, slowly enlarging cervical mass, and the median age of presentation is 45–54 years, with female predominance 2:1.[4],[5],[6]

The incidence of malignant form is 6% to 24% of nonadrenal paraganglia.[7] The risk of malignancy is more in young patients with heritable tumors. The distinction between benign and malignant form cannot be made on cytomorphology or histopathology. Malignant carotid body paraganglioma usually metastasizes to the regional lymph nodes, liver, bone, or lungs.[7] Our case presented with painless, progressive cervical lymphadenopathy, which on FNAC turned out to be an unsuspected case of malignant carotid body paraganglioma contrary to usual presentation of tumor itself presenting as a cervical mass.

The cytomorphological features are well established,[3],[8],[9] with smears showing cells arranged in loose cohesive clusters and singly with acinar/follicles/rosette formations. Tumor cells are round-to-oval, plasmacytoid, or spindle-shaped cells with moderate anisonucleosis. Fine and dusty chromatin with salt and pepper pattern is characteristic. Cells have abundant cytoplasm and indistinct cytoplasmic borders and may show red granules or vacuolization.

In the neck region, carotid body paraganglioma can be difficult to differentiate from thyroid neoplasms, neurogenic tumors, and metastatic carcinoma.[10] Acinar structures in paraganglioma can be mistaken for the follicles seen in follicular neoplasm of the thyroid. However, the identification of colloid is useful in such a setting. A misdiagnosis of the neurogenic tumor can occur if there is a predominance of ovoid- or spindle-shaped nuclei in a paraganglioma. The uniform and fine chromatin pattern of the nucleus in paraganglioma helps in distinguishing it from metastatic carcinoma.

Ancillary techniques are helpful for the confirmation of carotid body paraganglioma. It shows immunoreactivity for chromogranin, synaptophysin, neuron-specific enolase, and S-100.[11] Radioimaging studies, such as CECT and magnetic resonance angiography, and vascular imaging studies, such as Doppler ultrasound and selective digital subtraction angiography, are useful adjuncts to cytomorphology. These studies help in the exact localization of carotid body paraganglioma and also define their relation with major blood vessels.[12],[13] The diagnosis of malignant carotid body paraganglioma on FNAC of lymph node has been rarely reported. This case broadens the differential diagnosis of cervical lymphadenopathy. Authors also want to emphasize that aspiration cytology can be cost-effective and valuable tool to diagnose this rare tumor in unsuspected cases, which can be confirmed by radiological studies. It, thereby, helps the surgeon with the definite preoperative diagnosis so that the appropriate management can be planned for the patients with minimum complications.


 » Competing Interests Top


The authors declare that they have no competing interests.


 » Authorship Statement by All Authors Top


Each author has participated sufficiently in the work and takes public responsibility for the appropriate portions of the content of this article. SK carried out substantial contributions to conception and design, acquisition of data, and drafting the article. AA carried out substantial contributions to conception and design, acquisition of data, drafting the article, and revising it critically for important intellectual content.


 » Ethics Statement by All Authors Top


As this is case report without identifiers, our institution does not require approval from the Institutional Review Board (or its equivalent).


 » List of Abbreviations (In Alphabetic Order) Top


CECT - Contrast-enhanced computerized tomography

FNA - Fine-needle aspiration

MGG - May–Grunwald–Giemsa

MRA - Magnetic resonance angiography

PAP - Papanicolaou

USG - Ultrasonography.

 
 » References Top

1.
Barnes L, Eveson JW, Reichart P, Sidransky D, editors. World Health Organization Classification of Tumors. Pathology and Genetics of Head and Neck Tumours. Lyon: IARC Press; 2005. p. 362-3.  Back to cited text no. 1
    
2.
Lack EE, Cubilla AL, Woodruff JM, Farr HW. Paragangliomas of the head and neck region: A clinical study of 69 patients. Cancer 1977;39:397-409.  Back to cited text no. 2
    
3.
van den Berg R. Imaging and management of head and neck paragangliomas. Eur Radiol 2005;15:1310-8.  Back to cited text no. 3
    
4.
Hood IC, Qizilbash AH, Young JE, Archibald SD. Fine needle aspiration biopsy cytology of paragangliomas. Cytologic, light microscopic and ultrastructural studies of three cases. Acta Cytol 1983;27:651-7.  Back to cited text no. 4
    
5.
Williams MD, Phillips MJ, Nelson WR, Rainer WG. Carotid body tumor. Arch Surg 1992;127:963-7.  Back to cited text no. 5
    
6.
Gaylis H, Davidge-Pitts K, Pantanowitz D. Carotid body tumours. A review of 52 cases. S Afr Med J 1987;72:493-6.  Back to cited text no. 6
    
7.
Dickinson PH, Griffin SM, Guy AJ, McNeill IF. Carotid body tumour: 30 years experience. Br J Surg 1986;73:14-6.  Back to cited text no. 7
    
8.
Lee JH, Barich F, Karnell LH, Robinson RA, Zhen WK, Gantz BJ, et al. National cancer data base report on malignant paragangliomas of the head and neck. Cancer 2002;94:730-7.  Back to cited text no. 8
    
9.
Fleming MV, Oertel YC, Rodríguez ER, Fidler WJ. Fine-needle aspiration of six carotid body paragangliomas. Diagn Cytopathol 1993;9:510-5.  Back to cited text no. 9
    
10.
Handa U, Bal A, Mohan H, Dass A. Parapharyngeal paraganglioma: Diagnosis on fine-needle aspiration. Am J Otolaryngol 2005;26:360-1.  Back to cited text no. 10
    
11.
Das DK, Gupta AK, Chowdhury V, Satsangi DK, Tyagi S, Mohan JC, et al. Fine-needle aspiration diagnosis of carotid body tumor: Report of a case and review of experience with cytologic features in four cases. Diagn Cytopathol 1997;17:143-7.  Back to cited text no. 11
    
12.
Varma K, Jain S, Mandal S. Cytomorphologic spectrum in paraganglioma. Acta Cytol 2008;52:549-56.  Back to cited text no. 12
    
13.
Gong Y, DeFrias DV, Nayar R. Pitfalls in fine needle aspiration cytology of extraadrenal paraganglioma. A report of 2 cases. Acta Cytol 2003;47:1082-6.  Back to cited text no. 13
    


    Figures

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