A Case Report of Advanced Cervical Cancer in a Patient Non-compliant With Age-Appropriate Screening (2024)

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A Case Report of Advanced Cervical Cancer in a Patient Non-compliant With Age-Appropriate Screening (1)

Link to Publisher's site

Cureus. 2022 Jan; 14(1): e21744.

Published online 2022 Jan 30. doi:10.7759/cureus.21744

PMCID: PMC8890600

PMID: 35251816

Monitoring Editor: Alexander Muacevic and John R Adler

Shobha Mandal,A Case Report of Advanced Cervical Cancer in a Patient Non-compliant With Age-Appropriate Screening (2)1 Sohaib Shabih,1 Jagdesh Kumar,1 and Surendra Shah2

Abstract

Cervical carcinoma is one of the preventable malignancies in the United States. Age-appropriate screening has decreased the incidence of cervical cancer.A multitude of age-appropriate screening methods is available including Papanicolaou (Pap) smear cytology, human papillomavirus (HPV) DNA testing, and visual inspection tests.Patients who are not up to date with the screening can remain asymptomatic until the advanced stage like in the case of our patient. We present a59-year-old female, who came in with progressively worsening shortness of breath on exertion, chest tightness, significant weight loss, and vagin*l bleeding for the past six months. On investigations, she was found to have cannonball metastases in the lung. The patient remained critically ill during her course of hospital stay and eventually passed away.

Keywords: screening, pap smear, cannonball mass, lung metastasis, cervical carcinoma

Introduction

Cervical cancer isone of themajor causesof cancer-related death in women worldwide [1]. It is the fourth mostprevalentcause of malignancy in womenafter breast, colorectal, and lung cancer [2].The incidence ofcervical cancer and mortalityrate has declined by 70% in the United States since the 1950s because of age-appropriate screening[3]. Among the several risk factors, human papillomavirus (HPV) types 16, 18, 31, 33, and 45 are the leading cause of cervical neoplasia [4]. Other risk factorsare smoking, low socioeconomic status, early ageat the first coitus, multiple sexual partners, and multiparity[5].

Case presentation

A 59-year-old female with no significant past medical history, non-compliant with anyage-appropriatecancerscreening, presented to the Emergency Departmentwith progressively worsening shortness of breath on exertionwith productive cough andchest tightness for the past six weeks. She alsoendorsedmalaise, progressive fatigue,anorexia,chronic pelvicdiscomfort,and weight loss of70lbsin the last year. She denied any vagin*l bleeding ordischarge. She had not seen a physician inthe last eight yearsand never hada Papanicolaou (Pap) smear,mammogram,or colonoscopy done.

On arrival, the patient was in respiratory distress, requiring 6-8 L oxygen through nasal canula but otherwise, hemodynamically stable. On systemic examination,sheappeared cachectic, with bilateral coarse breath sounds on lung exam andrightlower quadrant tenderness on abdominal examination. Blood work showed leukocytosis(WBC count: 20K cell/Liter), lactic acidosis (4.6 mmol/L), hypercalcemia(serumtotal calcium12.6 mg/dl), elevated d-dimer(1.6mcg/mL). Urinalysis was significant for hematuria but negative for pyuria. Serum lipase and amylase levels were unremarkable.Acid-base gasshowed pH7.43/PCO2 40/ PO2 59. Computed Tomography (CT) abdomen pelvis with intravenous contrast showed cervical soft tissue mass measuring up to 7x7 cm with an ill-defined feature, suggestive of neoplasm (Figure ​(Figure11).

Figure 1

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CT abdomen pelvis (sagittal view) showing soft tissue mass involving the cervix with nonhom*ogeneous density suggesting an underlying cervical mass (black arrow)

CT ofthechestwas obtained, which showed multifocal mediastinal masses measuring approximately 3 cm in the pre-tracheal and 35 x 37 mm in the SUV carinal region, bilateral hilar adenopathy,numerousnodular masses throughout the lung, and 50%predominance of focal lung consolidation (Figure ​(Figure22).

Figure 2

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CT chest showing multiple lesions in the lung suggestive of metastasis (black arrows)

Coronavirus disease 2019 (COVID-19) test was done, which was negative. Infectious workup, including blood culture, sputum culture and gram stain, legionella, and pneumococcal antigen tests were obtained, and the patient was started on empiric broad-spectrum antibiotics. As there was concern about cervical cancer with metastasis to the lungs, she was seen bya gynecologist and was planned forabiopsyof the cervical mass. Hematology/oncology was on board as well andrecommended a biopsy of the cervical mass with cytology, and HPV testing. If the biopsy comes positive for cervical cancer, she was planned to be started on a cisplatin-based chemotherapeutic regimen with the addition of checkpoint inhibitor therapy if the programmed death-ligand 1 (PD-L 1) biomarker was positive.

During the hospital stay, the patient continued to have worsening hypoxemia, with alteration in her mental status, and eventually developed multiple organ failure with renal dysfunction, transaminitis, and lactic acidosis.She was placed on bilevel positive airway pressure (BiPAP),but her oxygen requirements continued to worsen.The patient was Do-Not-Intubate (DNI)/Do-Not-Resuscitate (DNR).Palliative medicinewas on board forgoals of care discussion due to the patient’s declining clinical condition. The familydecided toproceedwith comfort care measures and the patient passed away. We were not able to obtain the biopsy of the cervical mass as we wanted the patient condition to be more stable.

Discussion

The cervix is the lower part of the uterine cavity and iscovered with twotypes of cells: the glandular and the squamous cells. The junction of these two types ofcellsis known as the transformation zone.Mostcervical cancer originates from the transformation zone.Squamous cell carcinoma (95%) and adenocarcinoma (5%) are the two major histological types ofan epithelial tumor of the cervix, but in rare cases, the tumor can also be of a non-squamousvariant including adenosquamous carcinoma, neuroendocrine carcinoma, glassy cell carcinoma [6].

Metastasis in cervical cancer occursbyhematogenous and lymphatic spread. Lung, bone, liver, and brain are the most common organs of cervical cancer metastasis [7].The lung is the most common metastasis site of the cervix and metastasis to the lung occurs because of the hematogenousspread [8]. The incidence of lung involvement increasesstage-wise; 3.2% in stage I, 5.0% in stage II, 9.4% in stage III, and 20.9% in stage IV disease [9]. In the Surveillance, Epidemiology, and End Results (SEER) database study from 2020, it was found that patients with age greater than 65, non-squamous histology type cervical cancer, pelvic lymph nodes metastases, poor differentiation, other organ metastasiswere at higher riskfor lung metastasis [ 10].

Patients with early-stage cervical cancer are mostly asymptomatic but few of those who are symptomatic, present with lower abdominal pain, postcoital vagin*l bleeding,abnormal menstrual bleeding, post-menopausal bleeding,offensive vagin*l discharge, and dyspareunia [11]. vagin*l discharge may be watery,mucoid,or purulent. Patients in the advanced stage of cancer present with symptoms of urinary symptoms, lower abdominal pressure, hematuria, and hematochezia depending on the site of metastasis.

Screening strategies for cervical cancer include Pap smear testing alone, primary HPV testing alone,or co-testing (with Pap and HPV testing). For patients under 21, screening is notrequiredregardless of the ageof initiation of sexual activity.In patients between 21-29,screening isinitiatedat age 21 with cervical cytology every three years.Forpatients aged 30 to 65, either Pap testing aloneeverythree yearsor co-testing(PAPand HPV testing combined) every five years is recommended. For patients who are above 65,the decision tocontinue screeningdependsonwhether the patient has hadan adequateprior screening, life expectancy,and preferences in a shareddecision-makingdiscussion.Symptomatic patients should have Pap smear testing as part of a diagnostic workup, regardless of prior screeningresults [12].

It has been noted that more than half of patients who develop cervical cancer have not been screened adequately. Inmost ofthe patients with invasive cervical cancer, there was no Pap smear obtained in the past five years [13].Strategiesthat can be used to increase screening rates include actively inviting patients to scheduletimelyappointments for cervical cancer screening. Urgent care clinical visits can be used as an opportunity to screen patients who are unlikely to otherwisecomply withcervical cancer screening recommendations [14,15].

Cervical cancer can be diagnosed by colposcopy, fluorescence spectroscopy, molecular diagnostic methods like HPV DNA test, nuclear aneuploidy detection. Further testing with pelvicMRI and positron emission tomography-computed tomography (PET-CT)should be performed for locally advanced diseases. In patients with advanced cervical carcinoma, chest x-ray and brain CT can be done to rule out metastasis tothelung or brain [16].Early-stage cervical cancer has a good prognosis because of the advancement in the treatment includingsurgery, chemotherapy, or radiotherapy,but advanced cancer with metastasis has a poor prognosis with a median survival of 8-13 months [17].

Conclusions

In conclusion, most patients with advanced cervical cancer with lung metastasisare asymptomatic and are found to have incidental mass on routine chest x-rays or CT.As patients with advanced cancerhave a poor prognosis,age-appropriatescreening, early identification of patients athigh riskfor lung metastases, and early intervention can be lifesaving.

Notes

The content published in Cureus is the result of clinical experience and/or research by independent individuals or organizations. Cureus is not responsible for the scientific accuracy or reliability of data or conclusions published herein. All content published within Cureus is intended only for educational, research and reference purposes. Additionally, articles published within Cureus should not be deemed a suitable substitute for the advice of a qualified health care professional. Do not disregard or avoid professional medical advice due to content published within Cureus.

The authors have declared that no competing interests exist.

Human Ethics

Consent was obtained or waived by all participants in this study

References

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Articles from Cureus are provided here courtesy of Cureus Inc.

A Case Report of Advanced Cervical Cancer in a Patient Non-compliant With Age-Appropriate Screening (2024)

FAQs

What is the age limit for cervical cancer screening? ›

Updated cervical cancer screening guidelines from ACS recommend starting screening at age 25 with an HPV test and having HPV testing every 5 years through age 65. However, testing with an HPV/Pap cotest every 5 years or with a Pap test every 3 years is still acceptable.

At what age do you stop screening for cervical cancer? ›

If you've had a series of normal screening test results over a long period of time, then you can stop screening at age 65. If, in the past, you had an abnormal result or anything suspicious on a screening test, or had treatment for cervical cancer or precancer, then you should continue to be screened.

How long can you live with advanced cervical cancer? ›

more than 80 out of every 100 (more than 80%) will survive their cancer for 1 year or more after they are diagnosed. around 60 out of every 100 (around 60%) will survive their cancer for 5 years or more after diagnosis. around 50 out of every 100 (around 50%) will survive their cancer for 10 years or more after ...

Why is cervical screening not recommended under 25? ›

Cervical cancer is very rare in the under-25s, and cervical screening hasn't been shown to reduce cancer cases in this age group. Most cell changes in this age group will go away on their own. Screening individuals under the age of 25 can lead to treatment which may not be necessary.

Why no cervical screening after 65? ›

The screening programme stops then because individuals who have no HPV (human papillomavirus) at this time are very unlikely to go on to develop cervical cancer in later years. If you have never been for a cervical screening test you can ask at your GP surgery to have one, even if you are over the age of 65.

What is the age limit for via screening? ›

The test is most suitable for women aged 30–49 years, because most of the high-grade precancers of the cervix are detected in this age range. The test sensitivity of VIA (the capability of the test to correctly detect the precancers and cancers) decreases in postmenopausal women.

What is the exit age for cervical screening? ›

You should continue having your Cervical Screening Test every five years, up to the age of 74, even after you have been through menopause.

Does age matter in cervical cancer? ›

The majority of women who are diagnosed with cervical cancer are between the ages of 35 and 44. It rarely occurs in women younger than 20. While cervical cancer has the reputation for being a young woman's disease, more than 15 percent of cases occur in people over 65.

What age is high risk for cervical cancer? ›

Cervical cancer is most frequently diagnosed in women between the ages of 35 and 44, with the average age being 50. It rarely develops in women younger than 20. Many older women don't realize that they are still at risk of developing cervical cancer as they age.

Can you beat advanced cervical cancer? ›

Unfortunately advanced cancer can't usually be cured. But treatment might control it, help symptoms, and improve your quality of life for some time.

At what stage is cervical cancer untreatable? ›

Stage 4 cervical cancer is not curable in many cases. However, nearly 17 in 100 women will beat stage 4 cervical cancer. It is crucial to seek expert gynecologic oncology support in a high-quality healthcare system to determine the best course of action for you and your family.

What stage of cervical cancer is considered advanced? ›

Early-stage cervical cancer – this usually includes stages 1A to 1B1. Locally advanced cervical cancer – this usually includes stages 1B2 to 4A. Advanced-stage or metastatic cervical cancer – this usually means stage 4B.

What is the age limit for cervical screening? ›

All women and people with a cervix between the ages of 25 and 64 should go for regular cervical screening. You'll get a letter in the post inviting you to make an appointment.

How long does it take for HPV to cause abnormal cells? ›

For 9 in 10 of us, this happens within 2 years. Sometimes, HPV will remain in your body and it might cause cells to change. Changed cells may turn into cervical cancer over time if they persist and are not monitored or treated. Cervical screening (previously called a 'smear test') can find HPV and changed cells early.

Do I need a smear test if I am a virgin? ›

Yes. Doctors recommend routine cervical cancer screening, regardless of your sexual history. Tests used to screen for cervical cancer include the Pap test and the HPV test. Your doctor can help you understand whether one or both of these tests is best for you.

What is the target age for cervical cancer screening? ›

If a woman can be screened only once in her lifetime, WHO recommends the best age is between 35 and 45 years.

How often should a 70 year old woman have a Pap smear? ›

In general, women older than age 65 don't need Pap testing if their previous tests were negative and they have had three Pap tests, or two combined Pap and HPV tests, in the preceding 10 years. However, there are situations in which a health care provider may recommend continued Pap testing.

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