key: cord-0700205-8hewl77w
authors: Chakraborty, Rakashree; Pandya, Divya; Dausage, Priyanka; Chawla, Ashmita K.
title: Mucormycosis - The deadly fungus – A case report with dental perspective
date: 2022-03-18
journal: J Family Med Prim Care
DOI: 10.4103/jfmpc.jfmpc_1339_21
sha: db4d2733d788a059e027097061c6bdac64be3fd2
doc_id: 700205
cord_uid: 8hewl77w

Mucormycosis is a fungal infection caused by members of Mucorales and zygomycotic species. These are saprophytes known as Mucormycotina that grow from rotten matter or soils during the decomposition of soil. It has been seen affecting many COVID-19-affected patients recently in India. Mucormycosis can be diagnosed in six different sites depending on the immunological status and the site of the body affected. The six manifestations are rhinocerebral, pulmonary, cutaneous, gastrointestinal, and central nervous system or disseminated forms. Here, we present a dental case of mucormycosis or black fungus disease that has affected an immune-compromised patient who had suffered from COVID-19 2 months ago. Surgical debridement was done and the histopathologic study revealed fungal hyphae. Systemic antifungal therapy was administered that helped the patient to recover in 7-week time.

Introduction for a high index of suspicion for mucormycosis and the role of the dentist and primary care physicians in first identifying this disease and providing proper medical care to the patient to avoid any delay for better prognosis of the disease and prevent any complications. The ethical clearance was obtained from the institutional ethics committee of the university.

A 38-year-woman residing in Kolkata, West Bengal, reported to the dental outpatient department (OPD) with a chief complaint of tooth mobility in the upper left posterior region of the jaw with pain in the left eye for 5 days. Further history revealed that she suffered from COVID-19 2 months back and was admitted for the same for 6 weeks is now recovering. The patient gave a history of nasal stuffiness and breathing obstruction since then. The patient was a diabetic for 14 years and is under regular medication. On general examination, the patient was well oriented to time, place, and person. All the vital signs were within normal limits.

On extra-oral examination, there was a diffused swelling on the left side of the face extending anteroposteriorly from ala of the nose to the tragus of the ear and superoinferiorly from the inferior orbital margin to the upper lip line, measuring approximately 3 × 4 cm with a smooth surface, ill-defined margins with an erythematous overlying surface. On palpation, all inspector's findings were confirmed. Consistency was soft and tender with no bleeding or pus discharge extra orally.

On intra-oral examination, multiple irregular ulcers were present on the hard palate and the buccal vestibule bilateral of size 1.5 by 1 cm approximately [ Figure 1 ]. Pus discharge on manipulation was present. Tooth mobility, grade II was present from 23 to 27 regions. On palpation, the patient experienced pain on the left buccal vestibule. On intra-nasal examination, there was no evidence of any ulcers or any blood crustrations.

Based on the history and clinical examination, a provisional diagnosis of lethal midline granuloma was given. The patient was advised for blood examination, biopsy, and computed tomography (CT) of mid-face.

The blood examination revealed random blood glucose levels of 17 mmol/L, white blood cell count of 29 × 10 9 /L, neutrophil count of 82%, and a platelet count of 521 × 10 9 /L. The sodium level was 138 mm/L and the potassium level was 4.4 mmol/L. The renal function test revealed that the urea concentration was 5.2 mmol/L and the creatinine value was 120 µmol/L. The total serum protein was 64 g/L.

The CT scan of the patient showed soft tissue opacification in the left maxillary sinus along with mucosal thickening of the right maxillary sinus. There was marked soft tissue obliteration of the maxillary sinuses with bony destruction of the medial wall of the maxillary sinuses and nasal septum. The chest radiograph was not significant [ Figure 2 ].

After the biopsy, the histopathological report revealed non-septate hyphae, which are consistent with mucormycosis [ Figure 3 ].

The patient was then admitted immediately and was placed on intravenous antibiotics and intravenous fluid to prevent dehydration. Then, surgical debridement of necrotic tissues of the hard palate and an obturator was then delivered.

The management was a combined effort of the maxillofacial surgeon, the prosthodontic team, doctors from the department of ophthalmology, and the plastic surgery team. This was followed by the administration of systemic antifungals (ketoconazole) and amphotericin B. There has been much improvement observed in the patient in 7 weeks and is under regular check-ups.

Mucor mycosis is an opportunistic fulminant fungal infection caused by saprophytic fungi. [7] Rhizopus is the chief pathogenic mycotic organism in cases with rhinocerebral mucormycosis. [8] According to Brown, mucormycosis ranked third among opportunistic deep fungal infections, after candidiasis and aspergillosis. [8] It is transmitted by air-borne asexual spores and invades the tissue of patients with reduced host defenses via the respiratory tract, injured skin, or percutaneous route. They proliferate in the walls of blood vessels particularly paranasal sinuses (as was seen in our case), lungs, or gut, and cause infarction and necrosis of the tissue distal to the blocked vessels. Increased levels of free iron present in diabetic patients assist the growth of these organisms. [7, 9] The clinical presentations of mucormycosis are classified on the basis of anatomic localization, such as rhino-orbital-cerebral (ROCM), pulmonary, gastrointestinal, cutaneous, renal, and disseminated mucormycosis. [10] Rhino-orbital-cerebral mucormycosis originates in the paranasal sinus and gets extended to the brain. Extension to the eyes is possible leading to complete blindness. From the eyes, it can progress toward the central nervous system resulting in cranial neuropathies or cerebral abscesses. [7, 8] Oral mucormycosis without any other systemically compromised organs is quite uncommon. In our case, the patient had both a debilitating condition resulting from type-I diabetes and an acute inflammatory immune response due to COVID-19. [9] Cytopathology, histopathology, and cultures were done to confirm the diagnosis with contrast-enhanced CT, which is useful in defining the extent of the disease. Sinus CT is the preferred imaging modality, bony destruction is often seen only late in the course of the disease. Magnetic resonance imaging (MRI) is useful in identifying the intradural and intracranial extent of the disease, cavernous sinus thrombosis, or thrombosis of the cavernous portion of the internal carotid artery. Perineural spread of the disease can also be demonstrated with a contrast-enhanced MRI scan. [7] Aggressive medical treatment with conventional antifungals is the cornerstone for successful treatment. Polyenes such as amphotericin-deoxycholates are the primary therapeutic agents for mucormycosis. Close monitoring of serum electrolytes, such as polyenes, is essential. [7] Non-conventional therapeutic agents such as antidiabetics, iron-chelating agents, statins, granulocyte transfusions, cytokines, and hyperbaric oxygen have increased the survival rates up to 94%. [9, 11] Prevention always remains the gold standard. [12, 13] Conclusion Co-infections in patients with COVID-19 are an emerging concern, especially because of their complex diagnosis, severity, and increased mortality. Early diagnosis is the best way to manage oral mucormycosis, along with the reversal of the underlying predisposing risk factors and systemic disorders. Surgical debridement and prompt administration of antifungal agents give a better prognosis.

Nil.

There are no conflicts of interest. 

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