Case Report, Clin Oncol Case Rep Vol: 4 Issue: 11

Invasive Rhino-Orbital-Cerebral Mucormycosis In Sinonasal Neuroendocrine Carcinoma- A Case Report

Sherin Mary Philip^1*

¹Department of Pharmacology and Nutritional Sciences, Markey Cancer Center, University of Kentucky College of Medicine, Lexington, Kentucky

*Corresponding Author : Sherin M Philip
Department of Pharmacology and Nutritional Sciences, Markey Cancer Center, University of Kentucky College of Medicine, MS-301 Willard Research Building, Lexington, Kentucky
E-mail:

Citation: Philip MS (2021) Invasive Rhino-Orbital-Cerebral Mucormycosis In Sinonasal Neuroendocrine Carcinoma- A Case Report. Clin Oncol Case Rep 4:11.

Abstract

Keywords: Mucormycosis , Neuroendocrine carcinoma, Amphotericin B, Chemotherapy

Introduction Mucormycosis (previously called as Zygomycosis or phycomycosis)is an invasive infection caused by the widespread saprophytic organisms called Mucorale which has a potential to become life threatening. It was first described as Mycosis mucorina by Arnold Paltauf in 1885(1). It causes acute angioinvasive infection seen primarily in the immunocompromised individuals with seven genera within Mucorales namely Rhizopus, Mucor, Absidia, Saksenaea, Rhizomucor, Apophysomyces, and Cunninghamella documented as pathogenic, with the most common causative organism being Rhizopus species (2). The primary route of infection is by inhalation of asexual spores of Mucorales called sporangiospores , leading to invasive sinopulmonary infection in susceptible individuals with other occasional causes being ingestion of contaminated food or traumatic inoculation. From there, Central Nervous System (CNS) penetration occurs either by hematogenous spread or by direct cranial penetration from the paranasal sinuses (3, 4,). The definitive diagnosis depends on microbiological analyses of tissue obtained by biopsy or surgical debridement along with imaging with Computed Tomography (CT) or magnetic resonance imaging (MRI) scans to assess for sinus involvement or spread to contiguous structures . Successful treatment of mucormycosis requires surgical debridement of infected tissue, prompt institution of antifungal treatment, and correction of the underlying metabolic and immune derangement (4). Case History A 45 year old female was admitted with complaints of pain in the throat, backside, and abdomen along with fever on day 10 post chemotherapy. She was a known diabetic whose persisting nasal block, bleed was diagnosed with immunohistochemistry of excised mass from Septoplasty with Functional Endoscopic Sinus Surgery (FESS) to be positive for malignancy with histology favouring sinonasal neuroendocrine tumour (ki67 92%). She started chemotherapy with Etoposide ( 100 mg/m²) and Cisplatin ( 25 mg/m²) with Granulocyte Colony Stimulating Factor(GCSF) injection. On Day 10 post chemotherapy she was found to be neutropenic along with body ache and fever. Hence she was started on G CSF along with prophylactic antibiotics as well as antifungal prophylaxis. The blood and urine cultures were found to be sterile but G CSF had to be continued due to persistent neutropenia. Serum Galactomannan was found to be 2.35 while HRCT lungs taken did not suggest any abnormality besides possible atelectatic changes but antifungal prophylaxis was escalated to Voriconazole. On day18 post chemotherapy she developed pain in the right eye with periorbital swelling, difficulty opening eyelid along with headache. Suspecting Multiple cranial nerve palsy (3,6) or Tolosa hunt syndrome probably infiltration, neurologist initiated her with IV Methylprednisolone 125mg twice daily but the MRI of brain showed mucosal edema in right paranasal sinus and inflammatory changes in right orbit most likely to be infection hence MethylPrednisolone was stopped and she was started on ophthalmic steroids, ophthalmic antibiotic and eye lubricants. Nasopharyngoscopy was taken on day 20 post chemotherapy which suggested colonising fungal activity in the right nasal cavity thus requiring escalation to IV Posaconazole.On Day28 post chemotherapy,the MRI of brain and Peripheral Nervous System (PNS) taken to assess treatment progress demonstrated significant increase in right orbital cellulitis changes with bone erosion, poor enhancement and intracranial extension likely to be fungal sinusitis, right basifrontal leptomeningitis with small infarct requiring an emergency FESS with orbital exenteration of right eye . The histopathology confirmed invasive mucormycosis thus initiating IV liposomal Amphotericin B 250 mg(4mg/kg) once daily.On day3 of Amphotericin B she developed generalized maculopapular rash with pruritus and hypokalemia (2.8mEq/L) for which she was given antihistamine and topical moisturizers along with supplementation with intravenous as well as oral potassium till the end of treatment with Amphotericin B for a total course of 14 days after which she was restarted with IV Posaconazole. Discussion Mucormycosis commonly presents in five forms based on the area affected namely pulmonary, rhinocerebral,gastrointestinal, cutaneous, or the central nervous systems. The fungi penetrates the organs Philip SM, Clin Oncol Case Rep 2021, 4:11 Clinical Oncology: Case Reports Case Report A SCITECHNOL JOURNAL All articles published in Clinical Oncology: Case Reports are the property of SciTechnol and is protected by copyright laws. Copyright © 2021, SciTechnol, All Rights Reserved. through orbital, oral, nasal, or skin pathways and produce granulomatous, thrombotic and necrotic lesions, while the hyphae penetrate all normal structures. (4)Our case involves infection in the sinonasal area which extended towards the right eye classifying it broadly into rhinocerebral mucormycosis.Invasive mucormycosis in oncologic patients is usually seen in hematological malignancies, and is not that common in patients with solid tumors. Roden et al. in a study of 929 mucormycosis cases, state that only 7 out of 154 patients with malignancy related mucormycosis had non-hematological malignancy(NHM)(5)The common causes for mucormycosis include diabetes mellitus with or without diabetic ketoacidosis, malignancies (haematological and solid organ tumor), transplant recipients, corticosteroid therapy and neutropenia. In the Asian continent diabetes mellitus is the most common risk factor whereas haematological malignancies and transplantation are the major risk factors in European countries and the United States. Our case is of a diabetic patient with good glycemic control who had an unusually prolonged neutropenia period post chemotherapy for a non-hematological malignancy. Immunosuppressive therapy and high steroid dose in patients also make the patient susceptible to mucormycosis as corticosteroid impairs the macrophage and neutrophil function. The patient was also given steroids due to suspicion of neurological disorder which was then stopped (6).The patients with diabetes mellitus usually develop rhino-orbital-cerebral mucormycosis (ROCM) while patients with hematological neoplasms generally develop sino-pulmonary disease and trauma patients develop necrotizing skin and soft tissue infections.High residual morbidity and mortality is associated with rhinocerebral mucormycosis due to the angioinvasive nature of the fungus due to vascular occlusion and extensive tissue necrosis. Initial symptoms are usually those of a sinusitis preseptal or orbital cellulitis. Surgical intervention and debridement is the gold standard of treatment for eradicating the infection, and was associated with improved survival in several case series. In patients with rhino-orbital-cerebral mucormycosis (ROCM), sinus surgery is regarded as essential but extensive surgical debridement is difficult to achieve because important structures are often adjacent to necrotic tissues, particularly in sinonasal, rhinoorbital, and, especially, cerebral involvement. Our patient had undergone an emergency FESS with orbital exenteration of the right eye (4). Amphotericin B is considered the treatment of choice for mucormycosis with preference for its liposomal formulation since significant toxicity was associated with the high doses of amphotericin B deoxycholate (AmBd) needed to attain fungicidal effect against Mucorales species (4). Patients who respond to initial therapy with l- AmB may be switched to maintenance treatment with less toxic azoles like Posaconazole or Isavuconazole which may increase the likelihood of achieving effective drug concentrations in the brain. The optimal duration of treatment for CNS mucormycosis is unknown and must be weighed based on the extent of surgical debridement performed and the immune state of the patient as well as the affordability of the patient given the expense of antifungal treatment. European guidelines suggests to “continue treatment until complete response (on imaging) and permanent reversal of immunosuppression are achieved” but no prospective studies have been performed (2, 7).Amphotericin B crosses the blood–brain barrier poorly while concentrations of posaconazole are highly variable in treated patients (4). Our patient was started on Liposomal Amphotericin B upon report of mucormycosis for a course of 14 days which was then de-escalated to Posaconazole. A recent meta-analysis had 92 cases of mucormycosis in patients with prior antifungal prophylaxis with Voriconazole (52%), Fluconazole (25%), Itraconazole (7.6%), Posaconazole (5%) and Caspofungin (9.8%).An increase in frequency of mucormycosis cases after treatment with Voriconazole prophylaxis in HSCT patients was reported by Marty et al.,in 2016. Our case also had prophylactic therapy with Voriconazole prior to confirmation of mucormycosis from biopsy of the excised area. (6) Conclusion Mucormycosis is not only a disease of the immunocompromised host since a considerable number of cases are also seen in an immunocompetent host without any known underlying illness The overall rarity of this disease, and its often-rapid progression and severity impede treatment of the condition while the heterogeneity of clinical presentation, underlying comorbidities and treatments complicate data interpretation. Due to the increase in cases of breakthrough mucormycosis after general antifungal prophylaxis and the overall increase in cases in the population, anti-Mucorales prophylaxis studies should be given due importance, alongside the search for methods of faster diagnosis and treatment.