(Archives of Pathology and Laboratory Medicine[TA])
12,486 results
  • Paracoccidioidomycosis at Autopsy: A Case Series and Literature Review. [Journal Article]
    Arch Pathol Lab Med. 2026 Jun 30. [Online ahead of print]Sguassábia MK, Miguel M, … Silva-Vergara MLAP
  • CONCLUSIONS: This study, consistent with other autopsy series, confirms the systemic nature of this mycosis, particularly in HIV-infected patients. HIV infection appears to alter the natural history of paracoccidioidomycosis, resulting in a more acute, severe, and disseminated clinical course. All non-HIV-infected patients were diagnosed post mortem and had less extensive systemic organ involvement. The HIV-infected cases herein included represent the largest autopsy cohort of HIV-paracoccidioidomycosis coinfection reported to date.
  • In Reply. [Journal Article]
    Arch Pathol Lab Med. 2026 Jun 25; 150(7):499-500.Tazelaar HD, Aubry MC, … Myers JLAP
  • Immune-Mediated Necrotizing Myopathy: Evolving Insights, Current Understanding, and Future Directions for Myopathologic Diagnosis. [Review]
    Arch Pathol Lab Med. 2026 Jun 17. [Online ahead of print]Lee CM, Ferris SPAP
  • CONCLUSIONS: Recognition of IMNM as a distinct IIM subtype has advanced through the serologic discovery of myositis-specific antibodies and the 2016 European Neuromuscular Centre consensus on IMNM. Nevertheless, challenges persist, particularly in the accurate characterization of seronegative IMNM, limitations in the current clinical criteria for IIMs, and conflicting data on potentially useful markers like p62 immunohistochemistry. A multifaceted approach integrating clinical, serologic, and pathologic data is essential in the continued research to refine the myopathologic diagnosis of IMNM.
  • Intracholecystic Tubular Nonmucinous Neoplasm of the Gallbladder. [Review]
    Arch Pathol Lab Med. 2026 Jun 12. [Online ahead of print]Pehlivanoglu BAP
  • CONCLUSIONS: ICTNs, initially recognized by their distinctive morphology and growth pattern, have distinct clinicopathologic characteristics. They are unlikely to be diffuse and multifocal like ordinary intracholecystic papillary neoplasms (ICPNs), and they do not appear to confer the field risk that ICPNs do. Instead, they form solitary pedunculated polyps (and often appear as detached debris in the lumen) and occur in the background of uninvolved gallbladder. In fact, they appear to be arising in cholesterol polyps. By morphology and MUC6 expression they resemble pancreatic/biliary intraductal tubulopapillary neoplasms, and they have been also called "complex nonmucinous pyloric gland adenomas" in the past. Although their complexity warrants the diagnosis of high-grade dysplasia/carcinoma in situ (and they have been typically diagnosed as "tubular adenocarcinoma" in Asia and South America), ICTNs are invasion resistant, with no documented invasive carcinoma developing within this lesion to date. The presence of morules, which display nuclear β-catenin expression, places this lesion in the so-called BROCN family of tumors, which are believed to be hormonally driven. Further molecular studies are needed to explore the roots of their behavior.