Evidence map›Paper›PMID 42098856›Full record

ArticleJournal of medical case reports2026

Breaking the serologic rule: chronic hepatitis B with simultaneous HBsAg and anti-HBs positivity-a case report.

Ghada Mohamed Balah, Mohammed Salmen Bazuqamah, Eslam Ahmed Helal, Mohammad Aly Moharram, Hend Masoud Masoud, Amira Abdelfatah Soliman, Ali Ismail Yahya

Abstract readCase Reports
In one paragraph

Article in Journal of medical case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Ghada Mohamed BalahImmunology & Virology Laboratory Department, King Khalid Hospital, King Abdulaziz Road, 66261, Najran, Saudi Arabia. ghadabalah@gmail.com.ORCID http://orcid.org/0009-0000-9235-7979
Mohammed Salmen BazuqamahMicrobiology Laboratory Department, King Khalid Hospital, Najran, Saudi Arabia.
Eslam Ahmed HelalBiochemistry Laboratory Department, King Khalid Hospital, Najran, Saudi Arabia.
Mohammad Aly MoharramHematology Laboratory Department, King Khalid Hospital, Najran, Saudi Arabia.
Hend Masoud MasoudMicrobiology Laboratory Department, King Khalid Hospital, Najran, Saudi Arabia.
Amira Abdelfatah SolimanHematology Laboratory Department, King Khalid Hospital, Najran, Saudi Arabia.
Ali Ismail YahyaBlood Bank Laboratory Department, King Khalid Hospital, Najran, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic hepatitis B virus (HBV) infection continues to pose a significant global disease burden, because of its potential progression to liver cirrhosis and hepatocellular carcinoma (HCC). Worldwide, more than 250 million individuals are estimated to be living with chronic HBV infection. Under standard serologic interpretation, the presence of hepatitis B surface antigen (HBsAg) signifies ongoing infection, whereas antibodies to hepatitis B surface antigen (anti-HBs) are generally associated with viral clearance or protective immunity. The simultaneous presence of both markers is rare and may lead to misinterpretation of serologic results, particularly when identified incidentally during routine screening in a primary care settings. CASE PRESENTATION: We describe a 60-year-old Saudi woman with an asymptomatic chronic HBV infection incidentally identified during routine pre-colonoscopy screening in a primary care setting. Laboratory testing revealed reactive HBsAg, total anti-HBc positivity, reactive anti-HBs titer, and HBV DNA level was 275 IU/mL consistent with low-level viremia. Liver enzymes were mildly elevated on prior testing subsequently normalized on follow- up. Transient elastography demonstrated no evidence of hepatic fibrosis or steatosis. The patient had no history of HBV vaccination, blood transfusions, liver disease, or recognized high-risk exposures, including intravenous drug use or high-risk sexual or household contact.

conclusionThis case highlights a diagnostic pitfall in HBV serology, as concurrent HBsAg and anti-HBs positivity does not indicate viral clearance and may reflect immune escape mutations, viral heterogeneity, or host immune factors. Recognition of this rare serologic profile is particularly important for primary care physicians, as accurate interpretation requires integration of serologic, virologic, and clinical data, particularly in asymptomatic patients identified through routine screening. This ensure appropriate diagnosis, long-term surveillance, and risk stratification. Clinicians should remain vigilant when encountering this rare serologic profile to guide appropriate referral and follow-up.

Indexed as

Hepatitis B AntibodiesHepatitis B, ChronicHepatitis B Surface AntigensDNA, ViralFemaleHepatitis B virusHumansMiddle AgedDNA, ViralHepatitis B AntibodiesHepatitis B Surface AntigensAnti-HBsCase reportChronic hepatitis BConcurrent HBsAg and anti-HBsDiagnostic pitfallHBsAgHepatitis B virus DNA

Identifiers

PMID42098856
PMCPMC13220585

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