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Search Results for Dysplasia
Abstract Number: 413
Great Toes as the Diagnostic Secret for Fibrodysplasia Ossificans Progressiva
Hospital Medicine 2018; April 8-11; Orlando, Fla.
Case Presentation: A 12-year-old female presented to the ER with a 1-week history of painful swelling of her right upper back not alleviated by NSAIDs or warm packs. She denied a history of recent trauma or fever. She has a history of surgical removal of a cranial myofibroma at 5 months of age and persistent [...]
Abstract Number: 441
THE CASE OF THE MISSING MULTIMERS: ACQUIRED VON WILLEBRAND SYNDROME IN A PATIENT WITH HYPERTROPHIC CARDIOMYOPATHY
SHM Converge 2021
Case Presentation: An 81-year-old woman with a history of hypertrophic cardiomyopathy (HCM) and prior gastrointestinal (GI) bleeding of unknown origin in 2017 presented with lightheadedness and anemia after undergoing an ERCP the day before. She had multiple episodes of maroon-colored stool and melena while in the ED and was transfused one unit of packed red [...]
Abstract Number: 620
BEWARE OF RINGING BEADS! RARE CASE OF TRANSIENT ISCHEMIC ATTACK FROM FIBRO-MUSCULAR DYSPLASIS(FMD) OF CERVICO-CRANIAL ARTERIES
Hospital Medicine 2019, March 24-27, National Harbor, Md.
Case Presentation: Fibro-muscular dysplasia is a segmental, non-atherosclerotic, non-inflammatory vascular disease of unknown etiology usually found in small and medium-sized arteries. Renal arteries (60–75%) are most commonly involved, followed by the cervico-cranial arteries (25–30%). FMD of cervico-cranial arteries in absence of renal artery involvement is much rarer. We present a case of symptomatic fibro-muscular dysplasia [...]
Abstract Number: 809
OCCULT GASTROINTESTINAL HEMORRHAGE IN VALVULAR AORTIC STENOSIS: THE IDENTIFICATION OF HEYDE’S SYNDROME AND THE NECESSITY FOR ACTION
Hospital Medicine 2020, Virtual Competition
Case Presentation: An 84-year-old woman with a history of hypertension and aortic stenosis (AS) presented with progressive dyspnea on exertion and melanotic stools for one week. The patient was admitted twice recently for similar reasons. Physical exam was remarkable for pallor and a grade 4/5 systolic murmur at the cardiac base with radiation to the [...]
Abstract Number: 856
HEMATODIAPHYSEAL DYSPLASIA IN ADULT: GHOSAL SYNDROME – A CASE REPORT
SHM Converge 2024
Case Presentation: Ghosal hematodiaphyseal dysplasia (GHDD) is a rare autosomal recessive disorder presenting with myelophthisic anemia and distinctive bony changes. TBXAS1 gene encodes Thromboxane A synthase. In GHDD, dysregulation of TBXAS1 occurs and this increases prostaglandin synthesis and causes direct bone marrow injury. Here we report, a 31-year-old Southeast Asian female presented with bilateral knee [...]
Abstract Number: 876
TURNS OUT IT WASN’T JUST GAS
SHM Converge 2023
Case Presentation: A 7 year-old with hypohidrotic ectodermal dysplasia (ED) and recurrent sinusitis was admitted with diplopia, headaches, and fevers. In the preceding 2 months, he had multiple episodes of fever, nasal impetigo, and positive group A strep (GAS) throat swabs without pharyngitis. He was treated twice with azithromycin due to allergies to amoxicillin, cephalosporins, [...]
Abstract Number: 0909
RECURRENT UPPER GASTROINTESTINAL BLEEDING DUE TO SEVERE MITRAL REGURGITATION: A RARE CASE OF HEYDE’S SYNDROME
SHM Converge 2025
Case Presentation: A 75-year-old male with a history of gastrointestinal bleeding (GIB) due to angiodysplasia, aortic stenosis (AS) status post TAVR, moderate-severe mitral regurgitation (MR), CKD, GERD, and atrial fibrillation not on anticoagulation presented due to lightheadedness for 1 day when standing up, and fatigue for a few weeks. He also reported dark brown stools [...]
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  • NALTREXONE – INDUCED KRATOM WITHDRAWAL: A CALL FOR AWARENESS

  • A CASE OF AMANTADINE INDUCED LIVEDO RETICULARIS IN A PATIENT WITH MULTIPLE SCLEROSIS

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  • RECOGNIZING S1Q3T3 FOR WHAT IT IS: A NONSPECIFIC PATTERN OF RIGHT HEART STRAIN

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