Literature DB >> 27051712

Early investigation by fluor-18-fluorodeoxyglucose positron emission tomography of a metastatic basal cell carcinoma presenting with spinal cord compression: A case report.

Frédéric Arsenault1, Jean-Pierre Ayoub2, Anna Danilenko3, Luc Boucher1.   

Abstract

Entities:  

Keywords:  18F-FDG, fluor-18-fluorodeoxyglucose; BCC, basal cell carcinoma; CK, cytokeratin; CT, computed tomography; MRI, magnetic resonance imaging; PET/CT, positron emission tomography and computed tomography; basal cell carcinoma; imaging; nonmelanoma skin cancer

Year:  2015        PMID: 27051712      PMCID: PMC4808697          DOI: 10.1016/j.jdcr.2015.03.003

Source DB:  PubMed          Journal:  JAAD Case Rep        ISSN: 2352-5126


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Introduction

The incidence rate of nonmelanoma skin cancer in the United States is estimated at 2.8 million new cases each year, of which, 80% are of basal cell carcinoma (BCC) type. The real incidence of BCC is difficult to determine with precision, as they are usually excluded from most cancer registries. The cumulative lifetime risk of skin cancer is about 20% in the United States and even higher in countries with a greater proportion of fair-skinned individuals where the lifetime risk reaches up to 30% of the population. For both melanomas and BCC, the major etiologic factors include natural and artificial exposure to ultraviolet radiation.4, 5 BCC is usually treated by excision, with histologic margin control. Although this type of skin cancer has a high incidence, few will eventually show progression or recurrence. BCC shows a very low mortality rate. Metastases are infrequent, and BCC progression is usually characterized by a locoregional spread. However, recurring BCC is more difficult to treat and, if left untreated, can lead to deformities and debilitating effects, ultimately causing death.

Case report

A 33-year-old woman came to the emergency room with an acute and rapidly progressive onset of lower limb paresthesias and paraparesis. She reported insidious upper and middle back pain that had started a month prior. Her relevant medical history included a recently removed large right breast skin lesion at another hospital. The skin lesion was irregular and ulcerated. Histology of this lesion was unknown at the time of consultation at our center. There was a positive family cancer history (second-degree relatives with breast [40 years of age] and lung cancer [53 years of age]). With these rapidly evolving symptoms, cervical, thoracic, and lumbar spine magnetic resonance imaging (MRI) was conducted within a few hours. The initial evaluation was completed with a thoracic computed tomography (CT) scan. A pathological fracture of the third thoracic vertebrae with soft tissue extension into the spinal canal causing medullary compression was diagnosed. Fig 1 shows the patient's thoracic spine in sagittal view on the initial MRI, revealing a T3 pathological fracture and spinal cord compression, explaining the patient's lower limbs symptoms.
Fig 1

Sagittal view of the initial thoracic spine MRI. T2-weighted, turbo spin echo MRI sequence shows a pathological fracture of the vertebral body at the level of T3 (white arrow), with a lesion extending into the spinal canal, causing significant spinal cord compression.

In addition to the initial assessment, a positron emission tomography/CT scan (PET/CT) was performed 3 days after patient admission (Fig 2). The known T3 metastasis lesion was highly hypermetabolic (standardized uptake value max: 13.4). A cutaneous focus of fluor-18-fluorodeoxyglucose (18F-FDG) uptake on her right breast was seen, but considering a recent surgery, the differential diagnosis included a residual lesion, a metastatic lesion, or an inflammatory process secondary to the surgery. The PET/CT showed an 18- × 13-mm lymph node with intense 18F-FDG uptake (standardized uptake value max: 5.6) in close relationship with the right sternocleidomastoid muscle. A second and adjacent hypermetabolic lymph node located slightly posteriorly and a contralateral axillary lymph node were noted, which were both highly suspicious for cancer involvement and were both unsuspected on other imaging modalities. A left 8-mm pulmonary nodule showing high 18F-FDG uptake was also considered metastatic until proven otherwise. Mammogram did not show any suspicious lesion.
Fig 2

Axial screen capture of 18F-FDG PET/CT metabolic images and fusion images at the level of the T3 vertebrae metastasis (A), the right supraclavicular lymph node metastasis (B), the left axillary lymph node metastasis (note the visible right breast focus of uptake) (C), and the left lung metastasis (D).

A decompression surgery was performed 5 days after admission. The final histopathologic results confirmed a basal cell carcinoma metastasis with the following immunohistochemical profile: Cytokeratin (CK) AE1/AE3 positive, CK 5/6 positive, CK 20 negative, ER negative, and GCDFP-15 (BRST2) negative. This profile was not in favor of a metastatic neuroendocrine carcinoma such as a Merkel cell tumor or any other skin lesion. Both the vertebral lesion and initial skin lesion specimens were re-examined at another medical center by a neuropathologist and a dermatopathologist, who both confirmed a tumor of basal cell origin with identical histopathologic features. The initial tumor measured 12.6 × 9.4 cm, with perineural and lymphovascular invasion.

Discussion

Skin cancers are subdivided, in decreasing order of frequency, among basal cell carcinoma, squamous cell carcinoma, malignant melanoma, Merkel cell carcinoma, and other much less common histologic types. The most common subtypes are often the least aggressive ones and they are usually characterized by a very limited locoregional spread. Metastases occur much more often with Merkel cell carcinoma and malignant melanoma. A literature review on both Embase and Medline databases using the medical subject headings “basal cell carcinoma” and “spinal cord compression” yielded only 3 case reports. One of these described a spinal cord compression secondary to the direct extension of a local aggressive recurrence of a large BCC.9, 10, 11 Few articles address the value of PET/CT in the staging of BCC upon literature review with the medical subject headings “basal cell carcinoma” and “positron emission tomography.” Most frequently, the primary lesion of a metastatic BCC measures more than 4 cm in diameter, but primary BCCs as small as 1 to 2 cm have been reported to metastasize.12, 13 Lymph nodes, lungs, bones, and skin are the most frequent sites of secondary lesions. Perineural and lymphovascular invasion are associated with a higher risk to metastasize. This article is a case report of a patient with metastatic basal cell carcinoma presenting with spinal cord compression symptoms, in which PET/CT was used on the early initial workup. A large initial tumor-size BCC that was irregular and ulcerated was initially reported in our patient. In this specific case, the thoracic vertebra metastasis would have been identified before the pathological fracture if a PET/CT had been done at the time of the skin lesion removal surgery because of the high relative uptake value of the metastasis. Although metastatic BCC is a rare entity, it is nonetheless a tragic outcome for these patients. Clinical and histopathologic features of perineural and lymphovascular invasion are tumor features in patients who might benefit from an initial PET/CT investigation.
  13 in total

1.  Basal cell carcinoma (BCC) causing spinal cord compression.

Authors:  B Cohen; G Weiss; H Yin
Journal:  Dermatol Online J       Date:  2000-09

2.  Non-melanoma skin cancer and ten-year all-cause mortality: a population-based cohort study.

Authors:  Annette Østergaard Jensen; Anna Lei Lamberg; Jacob Bonde Jacobsen; Anne Braae Olesen; Henrik Toft Sørensen
Journal:  Acta Derm Venereol       Date:  2010-07       Impact factor: 4.437

Review 3.  Basal-cell carcinoma.

Authors:  Adam I Rubin; Elbert H Chen; Désirée Ratner
Journal:  N Engl J Med       Date:  2005-11-24       Impact factor: 91.245

4.  Metastatic basal cell carcinoma causing cord compression.

Authors:  J D Quin; C McNeill; A al-Dawoud; K R Paterson
Journal:  Scott Med J       Date:  1990-06       Impact factor: 0.729

5.  Early-onset basal cell carcinoma and indoor tanning: a population-based study.

Authors:  Margaret R Karagas; M Scot Zens; Zhigang Li; Therese A Stukel; Ann E Perry; Diane Gilbert-Diamond; Vicki Sayarath; Rita S Stephenson; Dorothea Barton; Heather H Nelson; Steven K Spencer
Journal:  Pediatrics       Date:  2014-07       Impact factor: 7.124

6.  Risk factors for basal cell carcinoma in the UK: case-control study in 806 patients.

Authors:  J T Lear; B B Tan; A G Smith; W Bowers; P W Jones; A H Heagerty; R C Strange; A A Fryer
Journal:  J R Soc Med       Date:  1997-07       Impact factor: 5.344

7.  Prevalence of a history of skin cancer in 2007: results of an incidence-based model.

Authors:  Robert S Stern
Journal:  Arch Dermatol       Date:  2010-03

8.  Clinical, histological and demographic predictors for recurrence and second primary tumours of head and neck basal cell carcinoma. A 1062 patient-cohort study from a tertiary cancer referral hospital.

Authors:  Athanassios Kyrgidis; Konstantinos Vahtsevanos; Thrasivoulos George Tzellos; Persa Xirou; Kyriaki Kitikidou; Konstantinos Antoniades; Christos C Zouboulis; Stefanos Triaridis
Journal:  Eur J Dermatol       Date:  2010-04-20       Impact factor: 3.328

9.  Metastatic basal cell carcinoma. Report of five cases.

Authors:  S N Snow; W Sahl; J S Lo; F E Mohs; T Warner; J A Dekkinga; J Feyzi
Journal:  Cancer       Date:  1994-01-15       Impact factor: 6.860

10.  Observation of a unique case of metastatic basal cell carcinoma found by radiographic evaluation in a patient with oculocutaneous albinism.

Authors:  Mickaila Johnston; Whitney Winham; Nicole Massoll; Jerad M Gardner
Journal:  F1000Res       Date:  2014-01-15
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