Rare disease

Successful pregnancy and delivery following surgical treatment of postmyomectomy uterocutaneous fistula
Mert Yesiladali, Erdinc Saridogan, Ertan Saridogan

BMJ Case Reports CP Dec 2019, 12 (12) e231594; DOI: 10.1136/bcr-2019-231594
Penile gangrene due to calciphylaxis: a multidisciplinary approach to a complex clinical challenge
Rowan David, Jake Nowicki, Jason Lee, Nicola Dean

BMJ Case Reports CP Dec 2019, 12 (12) e232138; DOI: 10.1136/bcr-2019-232138
Closed loop bowel obstruction secondary to left paraduodenal hernia (of Landzert)
Yeo Min Cho, Gamze Aksakal, Mohamed Ahmed Tawfik Ashour, Suzanne Moore

BMJ Case Reports CP Dec 2019, 12 (12) e232134; DOI: 10.1136/bcr-2019-232134
Tumour-induced osteomalacia due to an intra-abdominal mesenchymal tumour
Brijesh Krishnappa, Swati Ramteke Jadhav, Anurag R Lila, Tushar R Bandgar

BMJ Case Reports CP Dec 2019, 12 (12) e231728; DOI: 10.1136/bcr-2019-231728
Extrapulmonary sarcoidosis primarily presenting as cholestatic liver disease
Pieter De Mulder, Bert Maertens, Anne Hoorens, An Vonck

BMJ Case Reports CP Dec 2019, 12 (12) e232618; DOI: 10.1136/bcr-2019-232618
Superior vena cava syndrome due to mediastinal Gardner fibroma presenting as syncope
Robin George Manappallil, Harilal Nambiar, Neena Mampilly, Della Harigovind

BMJ Case Reports CP Dec 2019, 12 (12) e232433; DOI: 10.1136/bcr-2019-232433
Staphylococcus pseudintermedius catheter-related bloodstream infection after exposure to domestic dogs and a cat
Mark Anthony Diaz, Lindsay B Gardner, Claudia R Libertin

BMJ Case Reports CP Dec 2019, 12 (12) e231489; DOI: 10.1136/bcr-2019-231489
Rare case of trichobezoar causing pancreatitis in a young woman
Asma AlQaseer, Rawan A Rahman AlHarmi, Nooruddin AbuAli, Mohamed Ahmed

BMJ Case Reports CP Dec 2019, 12 (12) e229173; DOI: 10.1136/bcr-2018-229173
Fulminant Sphingomonas paucimobilis keratitis: case study and review of literature
Rinky Agarwal, Meghal Gagrani, Asmita Mahajan, Namrata Sharma

BMJ Case Reports CP Dec 2019, 12 (12) e231642; DOI: 10.1136/bcr-2019-231642
Partial deficiency of 17α-hydroxylase: a rare cause of congenital adrenal hyperplasia
Sílvia Cristina de Sousa Paredes, Olinda Marques, Marta Alves

BMJ Case Reports CP Dec 2019, 12 (12) e230778; DOI: 10.1136/bcr-2019-230778

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CLINICAL
- Anaesthesia (34)
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- Patients
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- Sociology
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- Statistics and research methods (1)
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Rare disease

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