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  Case reportActinomycosis of the parotid masquerading as malignant neoplasm.Bipin T Varghese1 1Department of Surgical Oncology, Regional Cancer Centre, Trivandrum 695011, Kerala, India 2Department of Imageology, Regional Cancer Centre, Trivandrum 695011, Kerala, India
BMC Cancer 2004, 4:7doi:10.1186/1471-2407-4-7 The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2407/4/7
© 2004 Varghese et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. Keywords: Actinomycosis, salivary gland, parotid, infection, tumour, pseudotumourAbstractBackgroundPrimary actinomycosis of the parotid gland is of rare occurrence and can mimic a malignant neoplasm both clinically as well as radiologically. Case presentationWe present here a case of primary actinomycosis of the parotid gland presenting with a parotid mass lesion with erosion of skull bones. ConclusionsClinical presentation of cervico-facial actinomycosis is characterized by the presence of a suppurative or indurative mass with discharging sinuses. The lesion demonstrates characteristic features on fine needle aspiration cytology and histology, however at times the findings are equivocal. BackgroundAlthough cervico-facial actinomycosis is well described, primary actinomycosis of the parotid gland is rare. Actinomycosis was considered to be the commonest of all deep mycotic infections or mycetomas in the past [1]. However now it is well established that it is a granulomatous lesion characterized by chronic suppuration usually caused by Actinomyces israelii which is a gram positive, non-acid fast, anaerobic, commensal bacteria within the oral cavity (tonsillar crypts and tartar of teeth). Unlike most of the mycotic infections, actinomycosis is not an opportunistic infection and the portal of entry is not through inhalation. Actinomycosis usually occurs in healthy individuals when the local condition favours its growth and very often, it is a mixed bacterial growth [2]. It commonly affects the facial soft tissue although it can spread to adjacent, salivary gland, bone, and skin of face and neck. Primary actinomycosis of the parotid gland is very rare and can mimic malignancy [3]. The diagnosis of this rare condition can be reasonably made empirically even when conclusive histological or microbiological evidence is not available. A case of primary actinomycosis of the parotid gland, which was diagnosed by its clinical features, radiological findings and its response to empirical medical management, is presented. Case presentationA 38-year-old man presented with a 5 × 4 cm rapidly progressive, firm swelling in the left parotid region with discharging sinuses on the overlying skin. The swelling was not painful and its size did not change with meals. There was no history of fever, malaise, cough, breathlessness, haemoptysis, trauma, surgery, recent tooth extraction, or dental infection. There was no history suggestive of Hansen's disease or sexual contact. He was not diabetic or immunocompromised. The swelling was confined to the parotid region (Fig 1, 2) rest of the face including submandibular region appeared normal. A 1.5 × 1.5 cm firm jugulodiagastric lymph node was palpable in the neck. Oral cavity, oropharynx, and indirect laryngoscopic examinations were normal. Mouth opening was adequate and there was no facial nerve palsy. Routine investigations including blood counts, erythrocyte sedimentation rate and chest X-ray were normal. ELISA test for HIV antibody was negative. The computerized tomographic (CT) scan showed a large parotid swelling extending to the base of skull with involvement of the skull bone (Figure 3). The mass lesion was seen extending into the parapharangeal space with thinning of the lateral wall of the maxilla on the left side (figure 4). The picture was suggestive of malignant neoplasm of the parotid gland.
Fine needle aspiration cytology (FNAC) of the parotid swelling and the neck node showed dense collections of neutrophils and macrophages with phagocytic activity, suggesting a chronic inflammatory process. Incision biopsy of the nodule with underlying parotid tissue showed salivary gland tissue with periductal lymphocytic infiltration in some of the ducts and adipose tissue, muscle bundles, sheets of lymphocytes, histiocytes, plasma cells, neutrophils and necrosis, suggestive of chronic sialadenitis. No fungal hyphae or bacteria or spores could be demonstrated in either the FNAC or in biopsy. AFB staining was negative. Based on the clinical, radiological and pathological findings a provisional diagnosis of chronic inflammatory pathology, probably actinomycosis was arrived at and the patient was started empirically on oral penicillin 500 mg 6 hourly for three weeks with complete clinical response (Fig 5, 6). The patient is disease free after and on regular follow-up after 2 1/2 years.
DiscussionThe commonest cause of a painless progressive swelling in the parotid region is the parotid neoplasms, the other causes being very rare (Table 1) [4-6]. A diagnosis can very often be made by clinical and radiological features followed by a fine needle aspiration cytology (FNAC). Actinomycosis of the parotid gland is rare and is often diagnosed by the presence of bacteria or spores in either FNAC or biopsy specimen. Microscopy may show features of granuloma with suppuration, chronic inflammatory cells, fibroblasts and giant cells. If suppuration is marked, the picture is that of an acute inflammation. It is uncommon to find colonies of microorganism in viable tissues although they are more easily demonstrated in discharge. Histological appearances are not characteristic and not much is expected from the biopsy [1]. However it can be diagnosed empirically, by mere exclusion, even in the absence of a conclusive pathological or microbiological report Table 1. Differential Diagnosis of Painless parotid mass Recognized routes of entry for cervico-facial actinomycosis include caries tooth, tooth extraction site and tonsils. It can also occur as a complication of trauma to respiratory and digestive tracts including operative procedures. Infection usually starts in the subcutaneous and submucous tissues and spreads by direct continuity [1,2]. Clinical presentation of cervico-facial actinomycosis is characterized by the presence of a suppurative or indurative mass with discharging sinuses. Pus from the discharging sinuses contains tiny yellow sulphur granules, which are diagnostic [1]. Common initial symptoms of infection including pain, fever, erythema, oedema, and suppuration may be absent [5]. Histopathological feature are similar to that of chronic inflammatory disease. FNAC and exfoliative cytology may demonstrate Curshmann's spirals and actinomycetes filaments in fortuitous cases [7]. Ultrasound and radiological investigations fail to differentiate them from malignancy, although conventional sialography or computerised tomography (CT) with sialography has been suggested to present a consistent pattern in infections [8]. A CT scan finding of soft tissue and bony invasion, simulating malignant neoplasm, helps in distinguishing actinomycosis from other suppurative or granulomatous masses. Drug of choice is penicillin or tetracycline. Anaerobic cultures may be helpful in selecting the appropriate antibiotic in refractory cases. Treatment is essentially medical with adjuvant surgical procedures like incision and drainage, and wound toilet [9-11]. A high index of clinical suspicion and negative tissue diagnosis of malignancy is the key to a presumptive diagnosis of this rare condition. Competing interestNone declared. Authors contributionsBTV carried out the literature search, prepared the draft manuscript and its subsequent revisions. PS, helped in preparing the manuscript and revised it for its scientific content. KR, did the imaging studies and contributed to the scientific content of the manuscript. MP contributed to the preparation of the manuscript and material for publication, edited the manuscript and coordinated the submission. All the authors were involved in the active patient management. All authors read and approved the final manuscript AcknowledgementWritten consent was obtained from the patient for publication of the patient's details. References
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