Publications by authors named "Sammer Elwasila"

osteomyelitis, in general, is a relatively rare manifestation compared to its bacterial counterparts. The mandible's involvement is rarer, lacking established management and fewer guidelines. Herein, we aim to illustrate the significant challenge in treatment, namely due to the persistent and resistant nature of -associated biofilm.

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Pure red cell aplasia (PRCA) is a rare hematologic disorder presenting with symptomatic normocytic anemia with preservation of other bone marrow cell lineages that may be acquired in adulthood due to malignancy, autoimmune disease, and infections. PRCA has been attributed to Epstein-Barr virus (EBV) in patients with underlying malignancy; however, we present a rare case of EBV-related PRCA in a previously healthy elderly male without an underlying malignancy who developed transfusion-dependent anemia that responded to glucocorticoids, rituximab, and intravenous immunoglobulins.

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BACKGROUND Leprosy, also known as Hansen's disease, is a neglected tropical disease with low prevalence in the United States. The disease's long incubation period can cause delayed presentation, and most affected individuals have a history of travel or work in leprosy-endemic regions. The immune response to Mycobacterium leprae determines the clinical characteristics of leprosy, with tuberculoid leprosy being characterized by well-defined granulomas and involvement of peripheral nerves.

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Article Synopsis
  • Monkeypox is becoming a significant global health concern due to its rapid spread and newly reported fatalities.
  • There is limited information on how monkeypox affects transplant recipients, as no case reports have been published regarding this group's clinical outcomes.
  • A case is presented of a kidney transplant recipient with severe monkeypox symptoms, including a widespread skin rash and other serious health issues, and the article discusses the use of tecovirimat, an antiviral treatment for monkeypox.
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Article Synopsis
  • spp. is a Gram-positive, partially acid-fast aerobic bacterium linked to infections in people with weak immune systems, affecting mainly the skin, lungs, and brain.
  • A case study of a 66-year-old immunocompetent man demonstrates the importance of correct diagnosis, as he was misdiagnosed multiple times and inappropriately treated after a gardening injury.
  • The case emphasizes the need for clinicians to be aware of rare causes of cellulitis, like nocardiosis, and the significance of thorough exposure histories for timely diagnoses.
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The species are Gram positive, coryneform bacteria that belong to the Actinobacteria phylum and have been linked to bacteremia in immunocompromised children. We present the first documented adult case of bacteremia. The patient was a 52-year-old woman with a history of recurrent infection, sinus tachycardia and high-risk AML who had been admitted one month prior to presentation for matched unrelated donor hematopoietic stem cell transplant with reduced intensity fludarabine-melphalan.

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Background: The criterion standard for the treatment of newly diagnosed primary central nervous system lymphoma (PCNSL) remains high-dose chemotherapy in conjunction with palliative whole-brain radiotherapy; however, there may be a role for novel combined approaches in immunocompromised patients.

Case Description: A 66-year-old man presented with acute cephalalgia, disorientation, and lethargy. His condition was evaluated in the emergency department, and he was admitted with probable hydrocephalus.

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Inflammatory bowel disease is a group of diseases that includes Crohn's disease (CD) and ulcerative colitis. CD is characterized as a chronic inflammatory disease of the gastrointestinal tract, ranging from the mouth to the anus. Although there are gross pathological and histological similarities between CD and Johne's disease of cattle, the cause of CD remains controversial.

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Aim: To investigate overlapping regions of the rpoB gene previously involved with rifamycin resistance in M. tuberculosis and seek correlation between rpoB mutations in clinical MAP strains with susceptibility to RIF and RFB.

Methods: We designed a molecular-based PCR method for the evaluation of rifabutin (RFB) and rifampicin (RIF) resistance based on probable determinant regions within the rpoB gene of MAP, including the 81 bp variable site located between nucleotides 1363 and 1443.

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