Histopathologic techniques are insufficient for distinguishing primary squamous cell carcinoma (SCC) from metastatic SCC, which is clinically important. A patient with SCC of the anus was found to also have SCC of the lung, and the question of metastatic versus synchronous primary diseases was raised. Immunohistochemical and hematoxylin and eosin (H&E) staining on sections of tissue could not discriminate between the two entities. Immunostain for p16 and chromogenic
Often clinical judgment has to be relied upon to differentiate between primary squamous cell carcinoma (SCC) of the lung and metastatic SCC of the anus. Hematoxylin and eosin (H&E) and immunohistochemical (IHC) staining on biopsy cannot distinguish the two entities. This case report exemplifies a woman with SCC of the anus with confirmation of lung metastasis using human papillomavirus type 16 (HPV-16) chromogenic
The patient is a 75-year-old woman diagnosed with a stage IV SCC of the anus. The patient reported hemorrhoidal problems which began to worsen in July 2003. A colonoscopy revealed the presence of grade 2 internal hemorrhoids, an anterior anal fistula, and a posterior anal papilloma. A fistulotomy and polypectomy were performed. The pathology report on the papilloma was unremarkable. She continued to have rectal bleeding and pain at the procedure site until a repeat colonoscopy was performed in March 2004, which revealed an anal fissure that was excised. At that time, the pathology report revealed an invasive poorly differentiated SCC with negative margins (Figure
Hematoxylin and eosin staining on anal fissure excision at 5x magnification (a) and 20x magnification (b). Immunohistochemical staining for p16 (c) and CISH for HPV-16 (d) were both positive.
Her past medical history is significant for osteoarthritis and depression, and she has never used tobacco. She underwent a computed tomography (CT) scan of the abdomen and pelvis, which reported mild wall thickening of the anorectal region without lymphadenopathy or extension of the tumor into the perirectal soft tissue. Chemotherapy and radiation therapy were both initiated, and she successfully completed both regimens 3 months later. During a follow-up appointment, a digital rectal exam revealed no palpable defects and complete healing of the prior procedure, and a colonoscopy performed in November 2004 was unremarkable. A CT scan of the chest performed within two years revealed an enlarging left lower lobe lung lesion. The lesion was positive on positron emission tomography (PET) scan, which was concerning for malignancy. The patient underwent a bronchoscopy and a left video-assisted thoracoscopy with wedge resection of the left lower lobe lung lesion in October 2009. The pulmonary tissue was formalin fixed and paraffin embedded using conventional methods. Four-micrometer sections of tissue were stained with H&E. Histopathologic examination of the lung lesion revealed poorly differentiated SCC with extensive necrosis; the tumor showed similar histopathologic findings to the lesion in the anus. Immunohistochemical staining of sections of the pulmonary and anal lesions was positive for p16 (Figure
To determine that the pulmonary SCC was a metastasis from the prior anal SCC and not a
Hematoxylin and eosin stain (a) and p16 immunohistochemical stain (b) on sections of lesion in left lower lobe wedge resection. CISH for human papillomavirus type 16 is seen at 400x original magnification (c) and 100x original magnification (d).
However, a definitive metastatic disease could not be distinguished from metachronous primary tumors; therefore, allelotyping using LOH was undertaken. Microdissection for the allelotyping was performed on conventional 4-micrometer-thick unstained histologic sections of formalin-fixed and paraffin-embedded tissue. Multiple microdissection targets were acquired from each tumor to determine intratumoral heterogeneity. Allelotyping consisted of both DNA sequencing for specific oncogene point mutation detection (k-ras-2) and a broad panel LOH cancer-associated marker. LOH was quantitative (polymerase chain reaction/capillary electrophoresis), allowing the detection of marker LOH and defining specific allele copy affected by imbalance and the temporal sequence of mutational acquisition over time. The marker panel targeted 1p, 3p, 5q, 9p, 10q, 17p, 17q, 18q, 21q, and 22q. Thresholds for accurate discrimination between true genomic loss and fluctuations from nucleic acid amplification were established. When one allele was absent in a microdissected neoplastic tissue section, this was recognized as a genomic deletion. Minor degrees of allele peak variation were corrected with algorithms dividing allelic ratios of tumor cells by those of nontumor cells. Normal ranges for each pair of alleles of given markers were based on a representative number of normal specimens from patients with no known neoplastic disease, which were used as controls.
Thresholds for minimal significant allelic loss were defined and applied. The proportion of cells with mutations in an individual microdissected sample was also assessed. To diagnose metastatic disease, determination of concomitant LOH affecting the same allele copy between the 2 tumor sites was necessary. Diagnosing metachronous primary tumors depended upon complete discordance with respect to temporal sequence of acquisition and/or specific allele copy involvement. The tumors are distinguished as primary or metastatic based on 3 levels of concordance. These include marker-affected tumors being considered concomitant if 50% or more of the same markers are mutated, the same gene copy is affected, and the temporal sequence of mutation is similar.
In the patient described in this case report, both tumors had identical allelic imbalance of 3p and 5q with the same allele copy affected in each specimen. The lung tumor had an additional 17p LOH. These data confirmed a metastatic anal SCC to the lung. The patient is currently clinically stable without signs of recurrent disease (Figure
Hematoxylin and eosin stained sections of tumors from the anal canal (left) and lung tumor (right) showing the sampled foci. Anal SCC sampled foci: 2T, 3T, and 4T; lung SCC sampled foci: 5T, 6T, and 7T; and lung normal: 1N for the loss of heterozygosity (LOH) allelotyping performed on lung tissue.
Squamous cell carcinoma of the anal canal is a rather rare phenomenon accounting for only 4% of all anorectal tumors. The majority of these tumors present as fissures, hemorrhoids, or anorectal fistulae [
The metastatic origin of the lung lesion is very important to differentiate from primary lung carcinoma for staging purposes, prognosis, and ultimately treatment modalities. Therefore, in this case, more advanced techniques had to be utilized to determine the site of origin, including CISH for HPV-16 and LOH allelotyping.
Human papillomaviruses are small DNA viruses that infect cutaneous or mucosal epithelium. HPV types 16 and 18 have been found to cause over 99% of cervical carcinomas, and these two types have been linked to carcinoma development in all internal organs with the exception of the heart and kidney [
If the anal SCC was positive for HPV type 16 and the pulmonary SCC was negative, that would indicate that the pulmonary SCC is a metachronous primary instead of metastasis. In this case, both the anal SCC and the lung were positive for p16 and HPV-16. These findings were very suggestive of a metastatic origin for the lung tumor. However, as HPV-16 is the most frequently detected HPV type in as many as 46% of primary lung SCC, the p16 and HPV-16 studies did not prove unequivocally that the pulmonary SCC was a metastasis from the anal SCC. These findings also did not prove that both tumors had a common clonal origin. Therefore, allelotyping for LOH was necessary to determine site of origin of the pulmonary tumor.
Most commonly, carcinomas can have areas on chromosomes in which the DNA is altered or sustains a LOH. Allelotyping is a process that involves withdrawing and amplifying the DNA to search for patterns of LOH or alteration [
H&E and immunohistochemical staining are very important in the process of identifying carcinoma. However, when treatment and prognosis are uncertain because the site of origin for a tumor is unknown, other techniques such as HPV typing by CISH and allelotyping for LOH can be very useful. These techniques can help to avoid misdiagnosis and mistreatment of neoplasia of metachronous tumors with the same histopathologic morphology.
The authors declare that there is no conflict of interests regarding the publication of this paper.