Contemporary Clinical Dentistry

: 2011  |  Volume : 2  |  Issue : 2  |  Page : 119--123

Rhinomaxillary mucormycosis: A palatal ulcer

Ranjana Garg1, Vivek Vijay Gupta2, L Ashok3,  
1 Department of Oral Medicine, BRS Dental College and Hospital, Panchkula, India
2 Department of Periodontics, BRS Dental College and Hospital, Panchkula, Haryana, India
3 Department of Oral Medicine, Bapuji Dental College and Hospital, Davangere, Karnataka, India

Correspondence Address:
Ranjana Garg
Department of Oral Medicine, C-53, Spangle Condos, Old Ambala Kalka Road, Vill. Gazipur, Zirakpur 140 603, Dist Mohali, Punjab


Rhinocerebral mucormycosis (zygomycosis) is an opportunistic fungal infection caused by saprophytic fungus. It involves several areas of the body, but the rhinocerebral form is most relevant to health care providers. Zygomycosis is associated with medically compromised patients. Our case reports an unhealed ulcer present over the palate of 15 days duration associated with swelling over the maxillary sinus region. This case is a blend of clinical, radiological, and histological manifestations of mucormycosis in a patient.

How to cite this article:
Garg R, Gupta VV, Ashok L. Rhinomaxillary mucormycosis: A palatal ulcer.Contemp Clin Dent 2011;2:119-123

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Garg R, Gupta VV, Ashok L. Rhinomaxillary mucormycosis: A palatal ulcer. Contemp Clin Dent [serial online] 2011 [cited 2020 May 31 ];2:119-123
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Rhinocerebral mucormycosis is a fatal opportunistic infection caused by a saprophytic fungus belonging to the group of Phycomycete. Paltauf in 1885 described the first case of this uncommon infection in human beings. Six clinical variants such as "rhinocerebral, pulmonary, cutaneous, gastrointestinal, central nervous system, disseminated type" have been recognized so far. Here, we present a histopathologically proven case of rhinomaxillary mucormycosis presented as a deep palatal ulcer in diabetic patients.

 Case Report

A 32-year-old man reported to the department with the chief complaint of pain and swelling below the left eye obstructing the vision from the same eye from past 1 month and an ulcer on the roof of mouth from the past 15 days. Pain was gradual in onset, severe, throbbing, continuous, and radiating to the left temporal region associated with swelling over the left maxillary sinus region that was insidious in onset and gradually progressed to the present size causing nasal obstruction and oedema around the left eye. There was a history of recurrent nasal discharge from the left nostril since 20 days. Around 15 days back, an ulcer developed over the palate which was rapidly increasing in size and was interfering with speech.

Patient's medical history revealed that he was uncontrolled type 1 diabetic patient from past 2 years and was on treatment (Inj. Mixtard 14 units per day). There was a family history of diabetes as patient's father had type 1 diabetes. The patient was tobacco chewer from past 15 years.

On general physical examination, the patient appeared febrile and the BP was recorded to be 160/90 mmHg.

On extraoral examination, a difuse swelling was appreciated over the left maxillary sinus region extending superoinferiorly from the left supraorbital margin to a line joining the left corner of mouth to the left ear and anteroposteriorly from nasal bridge to left ear. Overlying skin appeared normal with no secondary changes and on palpation was soft to firm in consistency with diffuse borders and tender with no local rise in temperature [Figure 1].{Figure 1}

On intraoral examination, an infiltrating ulcer approximately 3 × 4 cm 2 with irregular borders was appreciated over the hard palate. Ulcer was covered over by the necrotic slough and on the anterior aspect of the ulcer, part of the underlying bone was also exposed. Ulcer was nontender with few areas of erythema over the margins [Figure 2].{Figure 2}

Considering the patient's medical history and a rapidly proliferating ulcer denuding the underlying bone, a provisional diagnosis of deep mycotic infection of palate was made. The differential diagnosis of midline lethal granuloma and malignant ulcer was thought.

Later the patient was subjected to blood investigations which revealed raised ESR (34 mm/Ist hour) and random blood sugar around 220 mg%. Tridot and HBs test were negative.

Radiological investigations

Water's view revealed diffused radiopacity over the left maxillary antrum extending into left nasal cavity [Figure 3].{Figure 3}

CT scan in both axial [Figure 4]a and b and coronal sections [Figure 5]a and b revealed radiopacities along the walls of the left maxillary antrum with focal destruction of the bony walls extending into the left nasal cavity and floor of the left orbit.{Figure 4}{Figure 5}

The histopathological report suggests the presence of numerous aseptate fungal hyphae branching at 90° with neutrophillic infiltrate invading the smaller blood vessels (PAS staining) [Figure 6].{Figure 6}

Based on the above findings, final diagnosis of "Rhinomaxillary mucormycosis-A subdivision of rhinocerebral mucormycosis" was made.


The following treatments were carried out:

Surgical debridement of the necrotic tissue.Amphotericin B 1 mg/kg/day for 1 month.Nebulisation





It is a fatal opportunistic infection caused by a saprophytic fungus belonging to the group of Phycomycete. [1]Paltauf in 1885 described the first case of this uncommon infection in human beings. He coined the term mycosis mucorina which subsequently became mucormycosis.Disease received less recognition until 1942, when Gregory et al. reported three fatal cases of central nervous mucormycosis. [2]The disease may present with various manifestations, but there is a predilection for the paranasal sinuses. [3]


Organism is aerobic, but it can survive in vitro for 2-5 days. It is usually found in soil, bread moulds, decayed fruits, and vegetables. This organism can also be cultured from nasal cavity, throat, oral cavity, and stools of healthy patients. Organism belongs to:

CLASS - PhycomycetesORDER - MucoralesFAMILY - MucoraceaeGENERA - Rhizopus, Rhizomucor, Mucor, Absida

Clinical variants [4]

Eisenberg et al. described six clinical variants:

Rhinocerebral (Rhinomaxillary)PulmonaryCutaneousGastrointestinalCentral nervous systemDisseminated type

Adam in 1995 analyzed 116 cases and found:

39% - Rhinocerebral22% - Pulmonary type16% - Disseminated and cutaneous type4% - GIT.3% - Other locations.

Mucormycosis is the third most common invasive fungal infection, following aspergillosis and candidiasis, and accounts for 8.3-13.0% of all fungal infections found in autopsies of hematologic patients. [5]


Everyone is exposed to and inhales the spores; the nasal ciliary system transports these spores down in the pharynx to be cleared by the gastrointestinal tract. The spores inhaled by the lungs are cleared by the phagocytes. In the susceptible individuals [Table 1], the infection begins in the middle and inferior nasal turbinates. From the nasal cavity, the infection spreads to the paranasal sinus region and then to the retro-orbital region via direct extension or either through ethmoidal, lachrymal, and angular vessels. Infection can also spread to brain through the cribriform plate and the ophthalmic vessels. Following spread, function of the cranial nerves II, III, IV, and VI may be impaired and can lead to ptosis, proptosis, pupillary dilatation, visual loss, periorbital cellulitis, and numbness. [6]{Table 1}

Pathogenic relationship between diabetes and mucormycosis

Uncontrolled diabetes associated with ketoacidosis.

Abnormal polymorphonuclear chemotaxis.

Impair immunity.

Decreased polymorphonuclear phagocytic activity.

Oelaert and colleagues found that the patients with renal dialysis and iron over load patients treated with Deferoxamine B (Fe and Al chelator) are more prone to mucormycosis.

Rhizopus is more commonly associated with diabetes because of the active ketone reductase system it can thrive well in high glucose and acidotic conditions.

Clinical manifestations [7]

Age - any age group.Sex - both the sexes are equally affected.Site of invasion - Paranasal sinuses, lungs, kidneysMode of spread - either through direct extension or through blood vessels/lymph vessels.Sites involved - Palate being the most common site Buccal mucosa Upper and lower lip Mandible

In 1977, Eisenber et al. reported the first case of mandible mucormycosis.

In 1986, Brown and Finn reported the second case of mandible mucormycosis. The rhinocerebral form of mucormycosis is more common and is associated with homolateral facial palsy, anesthesia of the areas supplied by first and second division of trigeminal nerve.

Rhinocerebral mucormycosis is often associated with triad of symptoms

Uncontrolled diabetes mellitusPeriorbital infectionMeningoencephalitis

The 25% cases of the rhinocerebral mucormycosis form shows facial gangrene (Limongelli et al. 1975), the disease is known to present oral manifestations.

Intraorally, ulcer with raised erythematous borders with surface of the ulcer appearing black and necrotic with areas of denudation is seen.

Other associated signs and symptoms are:

Nasal obstructionBloody nasal dischargeFacial pain and headacheVisual disturbancesFacial paralysis

If there is cranial vault involvement, it can lead to blindness, lethargy, seizures or can even lead to death.

According to Moye and Cardill in 1980, black eschar formation is due to the thrombosis of blood vessels. Fungal hyphae have the affinity for blood vessels and invade the tissues. Direct penetration into blood vessels and growth of the fungus leads to thrombosis and necrosis of the adjacent tissues. [2]

Radiological features [8]

Nodular thickening of sinus mucosa, cloudy sinusitis without fluid levels, spotty destruction of bony walls of Paranasal sinuses were noted.

CT findings show opacificaton of paranasal sinuses, thickening of sinus mucosa, and erosions of the bony walls.


Surface swabs

Tissue biopsy

Culture and histological examination are imperative for the correct diagnosis of mucormycosis. Culture examination from the swab specimen can be negative for mucormycosis as it tends to invade deeply in the tissues. Therefore, it is mandatory to obtain the histological specimen as well culture specimen from the necrotic wound surface.

Stains used

Hematoxylin eosin stainPeriodic acid Schiff stainGridley's modificationGomori's methenamine silver nitrate

Culture media used are Sabourd's glucose agar. [9] Sporulation of fungal hyphae speciates for mucormycosis. Within 24-48 h of plating spores come to the surface of petridish.

Histological examination

Extensive areas of tissue necrosis and the presence of numerous fungal hyphae were noted. Hyphae are irregular, ribbon shape, aseptate with non-dichotomous branching at an obtuse angle and with areas of focal dilatations.

Width of hyphae - 15-20 μm

Length - 200 μm

Large necrotic areas with foci of suppuration, invasion of blood vessels, and their walls leading to thrombosis and tissue necrosis, and infiltration with PMN neutrophils and eosinophils.

Differential diagnosis

Wegener's granulomatosisMidline lethal granulomaNecrotizing sialometaplasiaSquamous cell carcinomaOther deep seated mycotic infections - Aspergillosis

In the later stage if palatal perforation occurs, differential diagnosis is [Figure 7]: [10],[11] {Figure 7}

Treatment [2]

In 1955, first cure of mucormycosis was reported by Harris.

Symptomatic treatment Specific treatment

Medical t/t Topical - Amphotericin B 50 mg of vial of AMB suspended in 10 ml of sterile water and diluted to 500 ml of glucose solution. Nebulisation - 4 ml in each nostril 4-6 times/day. Systemic - Hyperbaric oxygen 2 atm. For 1 h for 30 days. Amphotericin B 1.0-1.5 mg/kg/day. Liposomal AMB are the lipid formulations of AMB and can be prescribed safely to the patients with renal failure.Surgical t/t Caldwell Luc operation External ethmoidectomy Local debridement

Mortality rate [12]

Acc. To Adam et al.:16% - Cutaneous mucormycosis.67% - Rhinocerebral.83% - Pulmonary.100% - GIT and disseminated.


A non-specific palatal ulcer could well be the presenting sign of mucormycosis and it is therefore essential for dental practitioner be alert to early signs and symptoms of this disease, especially when evaluating the patients with the high-risk group.


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