Amy Brownlee
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Amy Brownlee has a total of 19 co-authors. Here are the top co-authors by number of shared publications:
Alena Arlova
Molecular Imaging Branch, National Institutes of Health, Bethesda, Maryland, USA
1 shared publication- Alfred Sidney Barritt
Division of Gastroenterology and Hepatology, University of North Carolina, Chapel Hill, North Carolina, USA
1 shared publication Alisa Siebrasse
Department of Gastroenterology and Hepatology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina
1 shared publicationBaris Turkbey
Molecular Imaging Branch, National Institutes of Health, Bethesda, Maryland, USA
1 shared publicationCurtis Lisle
KnowledgeVis, LLC, Maitland, Florida, USA
1 shared publication- Edwards Kasonkanji
University of North Carolina Project-Malawi, Lilongwe, Malawi
1 shared publication
Latest Publications
- Open Access
- 11 November 2026
- Published by BMJ in BMJ Connections Oncology
- Vol. 3 (1) , e000149
Triaging diffuse large B cell lymphoma and Burkitt lymphoma with AI in Malawi, using local patients and specimens for the development and testing of AI models
- 11 November 2026
- Published by BMJ in BMJ Connections Oncology
- Vol. 3 (1) , e000149
Open AccessTriaging diffuse large B cell lymphoma and Burkitt lymphoma with AI in Malawi, using local patients and specimens for the development and testing of AI models
- 1 October 2026
- Published by American College of Physicians in Annals of Internal Medicine: Clinical Cases
- Vol. 5 (10)
Variceal Bleeding: An Uncommon Presentation of Hepatic Sarcoidosis-Related Portal Hypertension
- 1 October 2026
- Published by American College of Physicians in Annals of Internal Medicine: Clinical Cases
- Vol. 5 (10)
Variceal Bleeding: An Uncommon Presentation of Hepatic Sarcoidosis-Related Portal Hypertension
- Open Access
- 1 January 2025
- Published by AOSIS in African Journal of Laboratory Medicine
- Vol. 14 (1)
Diagnostic adequacy of adult bone marrow biopsies in Malawi: A retrospective cohort study
Background: Bone marrow (BM) sampling is a critical component of clinical care, informing the diagnosis of benign and malignant haematologic disorders. Objective: We aimed to assess adequacy and characterise the spectrum of diagnoses rendered for BM samples reviewed at Kamuzu Central Hospital in Lilongwe, Malawi. Methods: We reviewed clinical and pathologic data from all adult BM specimens seen at Kamuzu Central Hospital from 01 June 2012, through 30 June 2024, and utilised R to summarise clinical and diagnostic data. Results: We identified 602 BM samples, most of which were biopsy-only specimens (n = 335, 56%). Most patients were male (n = 345, 57%), with a median age of 42 years. Of the 539 (90%) patients with known HIV status, 372 (69%) were HIV-uninfected. The most frequent indications for BM sampling were anaemia (n = 188, 31%) and cancer staging (n = 118, 20%). There was no documented indication for 72 cases (12%). Excluding BM samples obtained for cancer staging (n = 118, 20%), there were 403 (83%) diagnostic samples. Of these, 156 (39%) were malignant, with 50 (32%) acute leukaemias and 38 (24%) lymphomas. Conclusion: We found a high diagnostic yield (85%) of BM samples in this cohort, along with a considerable proportion of new cancer diagnoses (39%) in diagnostic samples taken for reasons other than cancer staging. Non-malignant diagnoses were predominant, yet resources for subcategorising these are limited in our setting. What this study adds: This study highlights the high diagnostic yield of adult BM samples at Kamuzu Central Hospital and characterises these diagnoses, revealing not only a substantial burden of malignancies but also important gaps in diagnostic capacity.
- 1 January 2025
- Published by AOSIS in African Journal of Laboratory Medicine
- Vol. 14 (1)
Open AccessDiagnostic adequacy of adult bone marrow biopsies in Malawi: A retrospective cohort study
Background: Bone marrow (BM) sampling is a critical component of clinical care, informing the diagnosis of benign and malignant haematologic disorders. Objective: We aimed to assess adequacy and characterise the spectrum of diagnoses rendered for BM samples reviewed at Kamuzu Central Hospital in Lilongwe, Malawi. Methods: We reviewed clinical and pathologic data from all adult BM specimens seen at Kamuzu Central Hospital from 01 June 2012, through 30 June 2024, and utilised R to summarise clinical and diagnostic data. Results: We identified 602 BM samples, most of which were biopsy-only specimens (n = 335, 56%). Most patients were male (n = 345, 57%), with a median age of 42 years. Of the 539 (90%) patients with known HIV status, 372 (69%) were HIV-uninfected. The most frequent indications for BM sampling were anaemia (n = 188, 31%) and cancer staging (n = 118, 20%). There was no documented indication for 72 cases (12%). Excluding BM samples obtained for cancer staging (n = 118, 20%), there were 403 (83%) diagnostic samples. Of these, 156 (39%) were malignant, with 50 (32%) acute leukaemias and 38 (24%) lymphomas. Conclusion: We found a high diagnostic yield (85%) of BM samples in this cohort, along with a considerable proportion of new cancer diagnoses (39%) in diagnostic samples taken for reasons other than cancer staging. Non-malignant diagnoses were predominant, yet resources for subcategorising these are limited in our setting. What this study adds: This study highlights the high diagnostic yield of adult BM samples at Kamuzu Central Hospital and characterises these diagnoses, revealing not only a substantial burden of malignancies but also important gaps in diagnostic capacity.