Rare disease

Adult-onset Still’s disease with concurrent thrombotic thrombocytopenic purpura: case report and literature review
Ryohei Kato, Tomoyuki Ikeuchi, Katsuyuki Tomita, Akira Yamasaki

BMJ Case Reports CP Sep 2020, 13 (9) e235786; DOI: 10.1136/bcr-2020-235786
Successful surgical resection of a rare case of a giant sacral chordoma: a multidisciplinary feat
Safwan Omar Alomari, Shadi Bsat, Mohammad Khalife, Ghassan Skaf

BMJ Case Reports CP Sep 2020, 13 (9) e235045; DOI: 10.1136/bcr-2020-235045
Down syndrome with co-occurring Marfan syndrome
Miao Wei, Natasha Lepore, Kelli Paulsen, Jonathan D Santoro

BMJ Case Reports CP Sep 2020, 13 (9) e235988; DOI: 10.1136/bcr-2020-235988
Solitary extramedullary plasmacytoma of the larynx: a rare cause of dysphonia
Hannes Hermann Brandt, Steffi Johanna Brockmeier, Nora Tetter

BMJ Case Reports CP Sep 2020, 13 (9) e234478; DOI: 10.1136/bcr-2020-234478
Adrenal medullary hyperplasia mimicking pheochromocytoma
Annalisa Montebello, Michelle Ann Ceci, Sandro Vella

BMJ Case Reports CP Sep 2020, 13 (9) e236209; DOI: 10.1136/bcr-2020-236209
Primary leptomeningeal T-cell lymphoblastic lymphoma: a rare cause of chronic meningitis
Arunmozhimaran Elavarasi, Rohit Bhatia, Sudheer Arava, Lalit Kumar

BMJ Case Reports CP Sep 2020, 13 (9) e236491; DOI: 10.1136/bcr-2020-236491
Eosinophilic colitis: an infrequent disease with difficult diagnose
Javier Páramo-Zunzunegui, Ignacio Ortega-Fernandez, Silvia Benito-Barbero, Laura Rubio-López

BMJ Case Reports CP Sep 2020, 13 (9) e235804; DOI: 10.1136/bcr-2020-235804
Congenital dysfibrinogenaemia presented with preterm premature rupture of the membranes and vaginal bleeding
Zaker I Schwabkey, Farrell C Sheehan, Courtney Bellomo, Mihir Raval

BMJ Case Reports CP Sep 2020, 13 (9) e235961; DOI: 10.1136/bcr-2020-235961
Bickerstaff’s brainstem encephalitis associated with anti-GM1 and anti-GD1a antibodies
Jonathan Cleaver, Richard James, Gurjit Chohan, Paul Lyons

BMJ Case Reports CP Sep 2020, 13 (9) e236545; DOI: 10.1136/bcr-2020-236545
Primary haemochromatosis resulting in dilated cardiomyopathy arising out of mutation in HJV gene in Indian patients: a rare scenario
Abhishek Goyal, Bishav Mohan, Kavita Saggar, Gurpreet Singh Wander

BMJ Case Reports CP Sep 2020, 13 (9) e235650; DOI: 10.1136/bcr-2020-235650

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CLINICAL
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- Statistics and research methods (1)
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Rare disease

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