Literature DB >> 24250107

Filarial abscess in the submandibular region.

Rupinder Kaur1, Kandathil Joseph Philip, Kumar R Laxman, Kanwal Masih.   

Abstract

Filariasis is a parasitic infectious disease caused by filarial nematode worms. These worms mainly dwell in subcutaneous tissues and lymphatics of the human host, with a predilection for lower limbs, retroperitoneal tissues, spermatic cord, and epididymis. Oral or perioral involvement of the filarial nematode is rare. This case report describes a filarial abscess in the right submandibular region. Fine needle aspiration cytology of the abscess revealed the presence of microfilaria of Wuchereria bancrofti species. The parasite was also present in the peripheral blood smear. Filarial infection presenting in this region is unusual and can cause diagnostic dilemma. The clinician can consider filariasis as one of the differential diagnosis while treating those abscesses in the orofacial region that are unresponsive to routine management, especially, patients hailing from endemic areas.

Entities:  

Keywords:  Filarial abscess; Wuchereria bancrofti; fine needle aspiration cytology; microfilaria; perioral filariasis

Year:  2013        PMID: 24250107      PMCID: PMC3830255          DOI: 10.4103/0973-029X.119769

Source DB:  PubMed          Journal:  J Oral Maxillofac Pathol        ISSN: 0973-029X


INTRODUCTION

Filariasis is a major public-health problem in the Asian and African subcontinent. Lymphatic filariasis is caused by the worms Wuchereria bancrofti, (W. bancrofti) Brugia malayi (B. malayi), and Brugia timori (B. timori). Among these W. bancrofti is the most prevalent parasite in India with a predilection for lower limbs, spermatic cord, and epididymis.[1] Breast,[2] thyroid,[3] body fluids,[45] and skin[6] are unusual sites for filariasis. Oral or perioral involvement is rare.[7] We present a patient with filarial abscess in the submandibular region.

CASE REPORT

A 25-year-old lady presented to dental out-patient services with swelling and pain in the right side of the face. Local examination showed a fluctuant swelling measuring 5 mm × 3 cm over the right side of the angle of mandible [Figure 1]. The swelling was warm and tender on palpation with signs of impending rupture. Clinical examination of the orofacial region did not reveal any odontogenic or non-odontogenic foci of infection. Patient's vitals were in the normal limits. All the hematological parameters were normal except for borderline leukocytosis and a low hemoglobin level. Incision and drainage (I and D) of the abscess was carried out under local anesthesia. As the patient was in her 12th week of gestation, antibiotics were prescribed in consultation with the gynecologist.
Figure 1

An indurated area (black arrow) approximately measuring 5 cm × 3 cm over the right angle region of mandible. The unresolved swelling seen after 2 weeks following incision and drainage (inset)

An indurated area (black arrow) approximately measuring 5 cm × 3 cm over the right angle region of mandible. The unresolved swelling seen after 2 weeks following incision and drainage (inset) On a follow-up visit after 2 weeks, a painless indurated swelling at the same site was noted [Figure 1, inset]. Pus culture carried out during the incision and drainage had not revealed any bacterial growth. As the condition was not resolving, a fine needle aspiration cytology (FNAC) was advised in consultation with the pathologist, to rule out tubercular infection. Aspirate from the swelling yielded purulent material. The smears were moderately cellular and showed abundant necrotic debris within which were seen polymorphs and histiocytes. One of the smears revealed the presence of a single microfilaria of W. bancrofti, which was rounded anteriorly and tapered posteriorly [Figure 2]. The caudal end of the microfilariae had a clear space free of nuclei. After the aspiration, the patient was admitted and a midnight blood sample was taken. The wet mount preparation showed motile microfilariae, which confirmed the diagnosis of filariasis.
Figure 2

Photomicrograph showing a microfilaria of Wuchereria bancrofti with rounded anterior and tapering posterior ends (MGG stain, ×400)

Photomicrograph showing a microfilaria of Wuchereria bancrofti with rounded anterior and tapering posterior ends (MGG stain, ×400) Since, the patient was in the first trimester of pregnancy, decision was taken to start the anti-filarial drugs after delivery.

DISCUSSION

Filariasis is common in tropical and subtropical areas of Africa, Asia, South and Central America. It is endemic in many parts of India. There are nine known filarial nematodes which use man as definitive host. Out of these, three worms live in lymphatics of the human host namely W. bancrofti, B. malayi, and B. timori. B. malayi is mostly confined to South-East Asia. B. timori is restricted to Indonesian islands. In India 99% of the cases are infected with W. bancrofti.[8] The life-cycle of the filarial worms (bancroftian and brugian filariasis) can be divided in to the mosquito phase and the human phase. Man is the definitive host and mosquito the intermediate host. The microfilaria of W. bancrofti and B. Malayi, both prevalent in India, display nocturnal periodicity as a part of the biological adaptation correlating with the nocturnal biting habits of the mosquito. Adult female worms of the above two mentioned species cannot be distinguished though, adult male worms show minor differences. Species diagnosis thereby is made on the basis of morphology of the microfilaria. Microfilariae of B. malayi are smaller than those of W. bancrofti, possess secondary kinks instead of smooth curve and unlike the latter, the tip is not free of the nuclei.[9] The common manifestations of lymphatic filariasis include, asymptomatic microfilaremia, early filariasis (filarial fever, lymphadenitis, lymphangitis, funiculitis, epididymitis, filarial orchitis, and filarial abscess), chronic obstructive filariasis (lymph node enlargement, thickened lymphatic channels, hydrocele, chyluria, chylocele, chylous ascitis, chylous diarrhea, elephantiasis, and lymphedema) and occult filariasis (tropical pulmonary eosinophilia, filarial arthritis, diffuse mesangial proliferative glomerulonephritis, pericardial, and endomyocardial fibrosis).[10] Perioral manifestations of lymphatic filariasis are extremely rare. Edematous swelling of lips and interdental papilla has been reported in a young patient with microfilaremia.[7] This case was unusual regarding clinical presentation, as the patient presented with an unresolved abscess in the orofacial region, clinically suspected to be of bacterial etiology, proven to be filarial abscess on FNAC. In addition, presence of microfilaria in the peripheral blood without associated eosinophilia is also a rare finding. Rare entities such as filarial abscess can be considered in the event of unresponsiveness to routine abscess management.
  5 in total

1.  Oral filariasis--a case report.

Authors:  Mohan Baliga; Arvind Ramanathan; Nakul Uppal
Journal:  Br J Oral Maxillofac Surg       Date:  2009-05-14       Impact factor: 1.651

2.  Microfilaria in thyroid gland nodule.

Authors:  Monisha Chowdhary; Sabeena Langer; Meenu Aggarwal; Chetna Agarwal
Journal:  Indian J Pathol Microbiol       Date:  2008 Jan-Mar       Impact factor: 0.740

3.  Microfilariae in cytologic smears: a report of six cases.

Authors:  R Varghese; C V Raghuveer; M R Pai; R Bansal
Journal:  Acta Cytol       Date:  1996 Mar-Apr       Impact factor: 2.319

4.  Microfilaria in a fine needle aspirate from a breast lump: a case report.

Authors:  P Sodhani; D A Murty; C S Pant
Journal:  Cytopathology       Date:  1993       Impact factor: 2.073

5.  Microfilariae of Wuchereria bancrofti in cytologic smears.

Authors:  A Walter; H Krishnaswami; A Cariappa
Journal:  Acta Cytol       Date:  1983 Jul-Aug       Impact factor: 2.319

  5 in total
  1 in total

1.  Filarial abscess: Aspiration of adult gravid female worm from submandibular region, an unusual presentation.

Authors:  Ruquiya Afrose; Mohammad Feroz Alam; Syed Shamshad Ahmad; Mohammed Naim
Journal:  J Cytol       Date:  2017 Jan-Mar       Impact factor: 1.000

  1 in total

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