Leptomeningeal carcinomatosis (LMC) is an end-stage disease with poor prognosis. This disease has not yet been reported with sinonasal carcinomatosis. We present a case of a patient who presented with posterior ethmoid/anterior cranial mass which turned out to be poorly differentiated squamous cell carcinoma (SCC). Later the patient presented with enhancement of the spinal roots and a lumbar puncture diagnosed the leptomeningeal spread of her primary disease. After intrathecal chemotherapy and palliative radiation, the patient failed to resist her disease seven months after the diagnosis. We present the first case report of leptomeningeal spread of sinonasal cancer. Although it seems rare, LMC should be on the differential of patients presenting with neurological deficits.
Leptomeningeal carcinomatosis (LMC), or carcinomatosis meningitis, is the infiltration of neoplastic cells into the leptomeninges. LMC is a relatively common and lethal complication caused by a variety of cancers, and is reported to occur in 1%-8% of patients with malignancies . LMC is most commonly a result of breast and lung cancer but can be caused by a variety of other solid tumors . Sinonasal carcinomas are rare and aggressive tumors of the nasal passage and paranasal sinuses that account for only 3%-5% of all head and neck cancers [3-5]. Due to the rarity of sinonasal carcinomas, LMC caused by a sinonasal carcinoma is exceedingly rare. We present, to our knowledge, the first reported case of LMC from a sinonasal squamous cell carcinoma (SCC).
A 66-year-old woman with a past medical history of hypertension presented with progressively worsening right eye visual acuity. Magnetic resonance imaging (MRI) revealed a large, heterogeneously enhancing mass centered in the right posterior ethmoid air cells, extending into the left ethmoid sinus and the right anterior cranial fossa, producing mass effect on the right optic canal and right optic nerve (Figure 1).
An endoscopic endonasal biopsy demonstrated a poorly differentiated Epstein-Barr virus (EBV) negative carcinoma. Histologically, the tumor was interpreted as a poorly-differentiated, SCC of the ethmoid sinuses with basaloid features, T4aN0M0 (Stage IVa, (American Joint Committee on Cancer (AJCC) 7th edition) (Figures 2-4).
Positron emission tomography/computed tomography (PET/CT) performed 15 days after the biopsy did not show any features of nodal or distant metastases. The treatment plan consisted of neoadjuvant fractionated external beam radiation with weekly cisplatin to be followed by definitive surgical resection.
The tumor initially responded well to the neoadjuvant radiation and chemotherapy, and decreased in size, from 2.3 x 2.7 cm in greatest dimension to 1.4 x 1.8 cm. However, approximately one month after finishing chemoradiation, and just days before scheduled surgical resection, the patient presented to the emergency department (ED) for low back pain and weakness that radiated to the bilateral lower extremities. An MRI of the cervical, thoracic, and lumbar spine revealed hyperintensities of multiple nerve roots within the cauda equina and T11-12 nerve roots (Figure 5).
The MRI was read as most consistent with arachnoiditis, although a differential of prior infection seqeuale and chronic subarachnoid hemorrhage, less likely LMC was provided. Given her disease history and concerning symptoms, a lumbar puncture (LP) was performed, and the cerebrospinal fluid (CSF) was positive for malignant cells, rendering the diagnosis of LMC (Figure 6).
Surgery was cancelled and her treatment plan was modified to intrathecal chemotherapy and palliative radiation. The patient ultimately succumbed to her disease seven months after initial diagnosis.
Central nervous system metastasis from head and neck cancers is rare. Additionally, only 2% of LMC arises from head and neck cancers. Diagnosis and treatment decisions for patients with leptomeningeal metastasis from solid tumors vary widely across Europe. Standardization of diagnosis and evaluation tools as well as controlled studies to improve the level of evidence for all therapeutic approaches to LM are required . Major favorable prognostic factors include excellent performance status, absence of serious fixed neurologic deficits, normal CSF flow scans, and absent or responsive systemic tumour. Aggressive therapy for this disorder is often accompanied by a necrotizing leukoencephalopathy which becomes symptomatic months after treatment with radiation and intrathecal methotrexate. As currently available therapies are toxic and provide limited benefits, novel approaches are being studied . Novel diagnostic approaches include the identification of biomarkers that may stratify the risk for developing leptomeningeal metastasis . It is important to keep in mind that the diagnosis can prove elusive and often requires a high index of suspicion to be established, as is highlighted in this case.
The primary diagnostic techniques in establishing a diagnosis of LMC include CSF cytology and MRI. It is important to note that a negative result on cytology does not exclude the diagnosis of LMC, and additional attempts at obtaining cytology should be made, as after three attempts, the sensitivity of cytology increases to ~90% . In the setting of equivocal imaging, clinical suspicion and decision-making become paramount. Maintaining suspicion for LMC in the setting of new-onset back pain despite inconclusive MRI prompted the lumbar puncture (LP) that identified LMC as the etiology of the patient’s pain. This diagnosis prevented the patient from undergoing surgical resection of the primary tumor, which would not have been curative and would have only exposed the patient to unnecessary morbidity.
This is a rare occurrence of leptomeningeal spread of SCC of the ethmoid sinus. This diagnosis should be on the differential diagnosis in patients presenting with new neurological deficits.
- Groves MD: Leptomeningeal disease. Neurosurg Clin N Am. 2011, 22:67-78. 10.1016/j.nec.2010.08.006
- Pavlidis N: The diagnostic and therapeutic management of leptomeningeal carcinomatosis. Ann Oncol. 2004, 15:285-291. 10.1093/annonc/mdh941
- Ansa B, Goodman M, Ward K, et al.: Paranasal sinus squamous cell carcinoma incidence and survival based on Surveillance, Epidemiology, and End Results data, 1973 to 2009. Cancer. 2013, 119:2602-2610. 10.1002/cncr.28108
- Peck BW, Van Abel KM, Moore EJ, Price DL: Rates and locations of regional metastases in sinonasal malignancies: the Mayo Clinic experience. J Neurol Surg B. 2018, 79:282-288. 10.1055/s-0037-1607288
- Sanghvi S, Khan MN, Patel NR, Yeldandi S, Baredes S, Eloy JA: Epidemiology of sinonasal squamous cell carcinoma: a comprehensive analysis of 4994 patients. Laryngoscope. 2014, 124:76-83. 10.1002/lary.24264
- Le Rhun E, Rudà R, Devos P, et al.: Diagnosis and treatment patterns for patients with leptomeningeal metastasis from solid tumors across Europe. J Neurooncol. 2017, 133:419-427. 10.1007/s11060-017-2452-6
- Grossman SA, Krabak MJ: Leptomeningeal carcinomatosis. Cancer Treat Rev. 1999, 25:103-19. 10.1053/ctrv.1999.0119
- Grewal J, Saria MG, Kesari S: Novel approaches to treating leptomeningeal metastases. J Neurooncol. 2012, 106:225-34. 10.1007/s11060-011-0686-2
- Subira D, Serrano C, Castanon S, et al.: Role of flow cytometry immunophenotyping in the diagnosis of leptomeningeal carcinomatosis. Neuro Oncol. 2012, 14:43-52. 10.1093/neuonc/nor172
Leptomeningeal Carcinomatosis from Squamous Cell Carcinoma of the Ethmoid Sinus: A Case Report
Ethics Statement and Conflict of Interest Disclosures
Human subjects: Consent was obtained by all participants in this study. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.
We thank Dr. Michael Glantz for his support and contributions to this publication.
Cite this article as:
Zammar S G, Hennessy M, Warrick J, et al. (July 30, 2019) Leptomeningeal Carcinomatosis from Squamous Cell Carcinoma of the Ethmoid Sinus: A Case Report. Cureus 11(7): e5281. doi:10.7759/cureus.5281
Received by Cureus: April 02, 2019
Peer review began: May 13, 2019
Peer review concluded: July 11, 2019
Published: July 30, 2019
© Copyright 2019
Zammar et al. This is an open access article distributed under the terms of the Creative Commons Attribution License CC-BY 3.0., which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.