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1.
Chest ; 158(2): e55-e58, 2020 08.
Article in English | MEDLINE | ID: mdl-32335068

ABSTRACT

We report the case of an 88-year-old man with coronavirus disease 2019 (COVID-19) who presented with ARDS and septic shock. The patient had exquisite BP sensitivity to low-dose angiotensin II (Ang-2), allowing for rapid liberation from high-dose vasopressors. We hypothesize that sensitivity to Ang-2 might be related to biological effect of severe acute respiratory syndrome coronavirus 2 infection. The case is suggestive of a potential role for synthetic Ang-2 for patients with COVID-19 and septic shock. Further studies are needed to confirm our observed clinical efficacy.


Subject(s)
Angiotensin II/metabolism , Angiotensin-Converting Enzyme Inhibitors/therapeutic use , Coronavirus Infections/drug therapy , Pneumonia, Viral/drug therapy , Respiratory Distress Syndrome/drug therapy , Shock, Septic/drug therapy , Aged, 80 and over , Angiotensin II/drug effects , Betacoronavirus , COVID-19 , Coronavirus Infections/complications , Coronavirus Infections/metabolism , Humans , Male , Pandemics , Pneumonia, Viral/complications , Pneumonia, Viral/metabolism , Respiratory Distress Syndrome/etiology , SARS-CoV-2 , Shock, Septic/complications , Shock, Septic/metabolism
4.
Mediterr J Hematol Infect Dis ; 5(1): e2013019, 2013.
Article in English | MEDLINE | ID: mdl-23505607

ABSTRACT

Intravascular large B cell lymphoma (IVLBCL) is a rare, aggressive extranodal B cell lymphoma, classified as a subset of diffuse B cell lymphoma. IVLBCL typically occurs in elderly persons and the clinical heterogeneity of the condition makes the diagnosis elusive in most cases. Most of the reported cases have been in the Asian population with the majority of the cases being diagnosed postmortem. We present a unique case of IVLBCL in a 65-year-old Caucasian male who presented with fever of unknown origin.

6.
Ann Saudi Med ; : 1-2, 2012 Jul 01.
Article in English | MEDLINE | ID: mdl-22750764

ABSTRACT

Intravenous immunoglobulin (IVIG), initially developed for immunodeficiency disorders, has now been used for multiple autoimmune diseases and infections. These are generally well tolerated, with few adverse effects. Acute kidney injury has been described in very rare instances. We report an interesting case of a 59-year-old African American male with a pertinent history of diabetes mellitus, hypertension, endocarditis, and peripheral vascular disease, who was diagnosed with post-transfusion purpura. He was then treated with IVIG and subsequently developed an acute worsening of renal function in a time span of 3 days. The etiology remained elusive even after an extensive workup. Renal biopsy was done finally, which showed findings suggestive of osmotic nephropathy that was traced to the sucrose used as a stabilizing agent in the IVIG. In light of the increasing use of IVIG, it is therefore highly recommended that clinicians are well aware of this side effect of IVIG.

8.
J Cancer Res Ther ; 8(1): 132-4, 2012.
Article in English | MEDLINE | ID: mdl-22531533

ABSTRACT

Leukemic and lymphomatous infiltration of the appendix is a rare complication. We present the case of a 31-year-old male with acute promyelocytic leukemia who developed acute abdomen on day 11 of induction chemotherapy with idarubicin and cytarabine. After appropriate work-up, a clinical diagnosis of acute appendicitis was made. Despite severe pancytopenia, he successfully underwent laparoscopic appendectomy. The final pathology revealed leukemic infiltration of the appendix. It is hypothesized that the leukemic infiltration may play a role in the development of acute appendicitis. Further, this case demonstrates the need to maintain a high index of suspicion and prompt surgical intervention for surgical pathologies in neutropenic patients.


Subject(s)
Appendicitis/complications , Appendicitis/diagnosis , Leukemia, Promyelocytic, Acute/complications , Leukemia, Promyelocytic, Acute/diagnosis , Leukemic Infiltration , Adult , Appendectomy , Appendicitis/surgery , Consolidation Chemotherapy , Humans , Induction Chemotherapy , Leukemia, Promyelocytic, Acute/drug therapy , Male , Treatment Outcome
9.
Blood Coagul Fibrinolysis ; 23(3): 238-40, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22356837

ABSTRACT

Venous thromboembolism is a rarely described complication of diabetic ketoacidosis (DKA). We describe a 21-year-old male patient with poorly controlled type 1 diabetes mellitus who was admitted with DKA, presumably secondary to noncompliance, whose clinical picture was complicated by generalized thrombosis involving multiple venous locations including renal vein, pulmonary vasculature, external iliac and common iliac veins. The patient had no family history of any coagulation disorders and a hypercoagulabilty work-up remained negative. The patient was subsequently anticoagulated with heparin and discharged home on warfarin. To the best of our knowledge, this is the first reported case of multiple venous thromboses occurring as a complication of DKA with no other risk factors. We also reiterate that although rare, venous thrombosis should always be considered as a potential complication of DKA.


Subject(s)
Anticoagulants/administration & dosage , Diabetic Ketoacidosis/complications , Venous Thrombosis/complications , Anticoagulants/therapeutic use , Diabetic Ketoacidosis/blood , Diabetic Ketoacidosis/drug therapy , Heparin/administration & dosage , Heparin/therapeutic use , Humans , Iliac Vein/physiopathology , Male , Patient Compliance , Pulmonary Veins/physiopathology , Renal Veins/physiopathology , Risk Factors , Venous Thrombosis/blood , Venous Thrombosis/drug therapy , Warfarin/administration & dosage , Warfarin/therapeutic use , Young Adult
12.
Blood Coagul Fibrinolysis ; 22(8): 746-8, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21885951

ABSTRACT

Mechanical valve thrombosis is a rare condition in an adequately anticoagulated patient in the absence of underlying thrombophilia. We report a case of a 76-year-old male with mechanical prosthetic mitral valve thrombosis as the presenting feature of polycythemia vera. The patient was treated with thrombolysis at the time of acute presentation and subsequently maintained on low molecular weight heparin, low-dose aspirin, phlebotomy and hydroxyurea. Hemoglobin, leucocytosis and platelet count were controlled for almost 4 years after which the patient suffered a second, fatal episode in the setting of therapeutic anti-Xa level. This case report highlights the thrombotic risks associated with polycythemia vera. The proposed mechanisms of hypercoagulability in polycythemia vera are reviewed. To the best of our knowledge, mechanical valve thromboses as the presenting feature of polycythemia vera has not been reported previously.


Subject(s)
Anticoagulants/administration & dosage , Mechanical Thrombolysis , Phlebotomy , Polycythemia Vera/blood , Thrombophilia/blood , Thrombosis/blood , Aged , Anticoagulants/therapeutic use , Aspirin/administration & dosage , Aspirin/therapeutic use , Factor Xa/metabolism , Factor Xa Inhibitors , Fatal Outcome , Heparin, Low-Molecular-Weight/administration & dosage , Heparin, Low-Molecular-Weight/therapeutic use , Humans , Hydroxyurea/administration & dosage , Hydroxyurea/therapeutic use , Male , Platelet Aggregation Inhibitors/administration & dosage , Platelet Aggregation Inhibitors/therapeutic use , Platelet Count , Polycythemia Vera/complications , Polycythemia Vera/drug therapy , Thrombophilia/complications , Thrombophilia/drug therapy , Thrombosis/complications , Thrombosis/drug therapy , United States
15.
World J Gastrointest Oncol ; 3(6): 99-102, 2011 Jun 15.
Article in English | MEDLINE | ID: mdl-21731909

ABSTRACT

We present an unusual case of renal cell cancer (RCC) which relapsed with duodenal metastasis and unveiled itself by gastrointestinal (GI) bleeding. An 80-year old Caucasian gentleman with history of renal cell cancer status post nephrectomy 11 mo previously, presented with syncope and melena. Computed tomography scan of the abdomen revealed heterogeneous soft tissue mass in the right nephrectomy bed invading the duodenum. Upper GI endoscopic biopsy confirmed the presence of recurrent renal cell cancer. However, due to extensive metastatic disease, the patient was placed on palliative chemotherapy as surgical options were ruled out. Our case report reiterates the fact that renal cell carcinoma can recur with gastrointestinal manifestations and, although a rarity, it should be considered in a patient with a history of malignancy who presents with these symptoms.

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