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1.
Urol Oncol ; 41(8): 359.e15-359.e23, 2023 08.
Article in English | MEDLINE | ID: mdl-37344326

ABSTRACT

BACKGROUND: Penile cancer accounts for less than 1% of male cancers in the United States. Localized disease, particularly T1 tumors are potentially curable with local therapy. We present the racial differences in survival outcomes for T1, penile cancer from the SEER database. METHODS: From 2004 to 2016 all men with T1, N0, M0 penile cancer in the SEER-18 database were included. Kaplan-Meier analysis and multivariable Cox-Regression analysis were conducted to investigate prognostic variables for cancer specific survival (CSS). RESULTS: A total of 4,406 men were identified with penile cancer; 1,941 men had T1 disease. The Kaplan-Meier (KM) analysis showed those with primary site surgery had better 5-year CSS compared to those without primary site surgery (P <.0001) and a significant difference in CSS based on race (P= 0.0078). On multivariable analysis, Hispanic individuals had worse CSS (HR 1.92; P = 0.0057) compared to the White men. Black men were also found to have a poor CSS however this was not statistically significant (HR 1.53, P = 0.118). Men with penile cancer who had either penectomy (HR 0.45; P = 0.006) or penile preservation surgery (HR 0.25; P< 0.001) had improved CSS. CONCLUSION: Racial disparities in CSS exist among men with in early-stage penile cancer. KM analysis showed significant differences in CSS by race and in those receiving primary site surgery. On multivariable analysis, the CSS is worse in Hispanic compared to White men. There is a trend towards worse CSS in Black men however this was not statistically significant.


Subject(s)
Penile Neoplasms , Humans , Male , Hispanic or Latino , Neoplasm Staging , Penile Neoplasms/surgery , Prognosis , Race Factors , SEER Program , United States/epidemiology , White , Black or African American
2.
Res Pract Thromb Haemost ; 6(2): e12688, 2022 Feb.
Article in English | MEDLINE | ID: mdl-35356668

ABSTRACT

Background: Acquired hemophilia A (AHA) is a disease caused by antibody formation inhibiting the function of factor VIII, causing bleeding. Recombinant porcine factor VIII (rpFVIII) escapes human FVIII antibody recognition and can provide life-saving hemostasis. However, the development of antibodies against pFVIII can limit its use. We report two cases in which loss of response to rpFVIII occurred, likely because of inhibiting antibodies. In case 1, the patient achieved hemostasis but lost response to rpFVIII within a few days. In the second case, rpFVIII controlled bleeding but the patient experienced diminishing half-life of rpFVIII infusions over time, necessitating a switch to emicizumab which provided lasting hemostasis. Key Clinical Question: Based on our experience with these cases, we reviewed the available literature regarding the use of rpFVIII in AHA. The Key Clinical Question was to determine how often inhibitors were associated with rpFVIII treatment failure. Clinical approach and conclusions: We identified 43 AHA patients across five studies who were treated with rpFVIII. Twenty-two patients (51%) developed pFVIII inhibitors and seven cases (16%) reported loss of efficacy associated with an inhibitor. In conclusion, rpFVIII can be a life-saving therapy in AHA. However, clinicians should be aware that pFVIII antibody development can reduce the efficacy and duration of response. Recombinant pFVIII's limitations support the utility of further investigation of alternative therapies such as emicizumab in early AHA management.

4.
BMJ Case Rep ; 13(6)2020 Jun 11.
Article in English | MEDLINE | ID: mdl-32532916

ABSTRACT

A 60-year-old woman presented with melena for 2 weeks. She had undergone hysterectomy and bilateral salpingo-oophorectomy to treat clear cell endometrial carcinoma 10 months before the presentation. She was anaemic and tachycardic; abdominal CT scan revealed a large duodenal mass. Her gastrointestinal bleed was not amenable to endoscopic intervention, so she had emergent laparotomy, pancreaticoduodenectomy with duodenal mass excision. Histopathology confirmed that the duodenal mass was a metastatic deposit from her clear cell endometrial cancer. Postoperatively, she was frail and chose hospice care and she died 90 days postoperatively. Clear cell endometrial cancer is a rare subtype of endometrial cancer, that has a worse prognosis compared with the more common endometrioid subtype. The duodenum is a rare site for metastatic endometrial cancer, and we report this case to alert clinicians to the possibility of metastases to the small intestine in patients with clear cell endometrial cancer.


Subject(s)
Adenocarcinoma, Clear Cell , Duodenal Neoplasms , Endometrial Neoplasms , Hysterectomy , Melena/diagnosis , Pancreaticoduodenectomy/methods , Salpingo-oophorectomy , Adenocarcinoma, Clear Cell/pathology , Adenocarcinoma, Clear Cell/surgery , Diagnosis, Differential , Dissection/methods , Duodenal Neoplasms/pathology , Duodenal Neoplasms/physiopathology , Duodenal Neoplasms/secondary , Duodenal Neoplasms/surgery , Endometrial Neoplasms/pathology , Endometrial Neoplasms/surgery , Fatal Outcome , Female , Hospice Care/methods , Humans , Hysterectomy/adverse effects , Hysterectomy/methods , Laparoscopy/methods , Melena/etiology , Middle Aged , Neoplasm Staging , Radiography, Abdominal/methods , Salpingo-oophorectomy/adverse effects , Salpingo-oophorectomy/methods , Tomography, X-Ray Computed/methods
5.
J Multidiscip Healthc ; 12: 471-477, 2019.
Article in English | MEDLINE | ID: mdl-31417270

ABSTRACT

Plummer-Vinson syndrome is a rare condition associated with dysphagia, iron deficiency, and esophageal webs. Data regarding this condition is limited to mostly case reports and a few small cohort studies. Although most cases have a benign and indolent course, the risk of malignancy warrants long-term surveillance. A multidisciplinary approach among healthcare providers is of the utmost importance in the management of this condition.

7.
F1000Res ; 7: 520, 2018.
Article in English | MEDLINE | ID: mdl-30135728

ABSTRACT

Kikuchi-Fujimoto disease is a form of a benign necrotizing lymphadenitis which is most commonly misdiagnosed as tuberculosis and or lymphoma, usually more common among young adults in Asia. It is a benign disease but can mimic a lot of other disease processes spanning infectious, rheumatologic and even hematologic malignancies. Our patient presented with prolonged fever and lymphadenopathy. Initial considerations were lymphoma and a nonspecific viral infection. A CT scan showed diffuse cervical lymphadenopathy with lacrimal gland involvement. An excisional lymph node biopsy was done which revealed Kikuchi disease. Patient was given steroids with immediate response with defervescence. Kikuchi is a disease with many mimics and a complete workup is needed to exclude serious disease like malignancy.


Subject(s)
Histiocytic Necrotizing Lymphadenitis/diagnosis , Biopsy , Diagnosis, Differential , Female , Glucocorticoids/therapeutic use , Histiocytic Necrotizing Lymphadenitis/blood , Histiocytic Necrotizing Lymphadenitis/diagnostic imaging , Histiocytic Necrotizing Lymphadenitis/drug therapy , Humans , Prednisone/therapeutic use , Tomography, X-Ray Computed , Young Adult
9.
BMJ Case Rep ; 20172017 Mar 17.
Article in English | MEDLINE | ID: mdl-28314808

ABSTRACT

Diffuse idiopathic skeletal hyperostosis (DISH) is a non-inflammatory condition characterised by calcification and ossification of the vertebral ligaments. It is most commonly seen to affect the thoracic and lumbar vertebrae and is usually seen among elderly men. The cause of this condition is unknown. Risk factors include male gender, obesity, diabetes and advancing age. The majority of these cases are found incidentally on imaging and patients are generally asymptomatic. Cervical DISH is less common than its thoracic and lumbar counterparts. When symptomatic, it can cause dysphagia or sometimes airway compromise. If this happens, surgical intervention should be performed. Although a rare cause of dysphagia, DISH is easily diagnosed with imaging. When identified, surgical decompression produces very good clinical outcomes.


Subject(s)
Deglutition Disorders/etiology , Hyperostosis, Diffuse Idiopathic Skeletal/complications , Aged , Cervical Vertebrae/diagnostic imaging , Deglutition Disorders/diagnostic imaging , Humans , Hyperostosis, Diffuse Idiopathic Skeletal/diagnostic imaging , Hyperostosis, Diffuse Idiopathic Skeletal/surgery , Male
10.
BMJ Case Rep ; 20172017 Feb 06.
Article in English | MEDLINE | ID: mdl-28167689

ABSTRACT

Apical hypertrophic cardiomyopathy (Yamaguchi syndrome) is a rare subtype of hypertrophic cardiomyopathy. The syndrome is more common in Japan where it was first described. Outside Asia, it is a very rare cause of hypertrophic cardiomyopathy. Apical hypertrophic cardiomyopathy is usually detected incidentally and has a good long-term outcome. We present a case of apical hypertrophic cardiomyopathy in an African-American patient manifesting as atrioventricular nodal re-entrant tachycardia.


Subject(s)
Black or African American , Cardiomyopathy, Hypertrophic/diagnosis , Tachycardia, Atrioventricular Nodal Reentry/diagnosis , Cardiomyopathy, Hypertrophic/surgery , Catheter Ablation/methods , Diagnosis, Differential , Electrocardiography , Humans
11.
Dement Geriatr Cogn Disord ; 43(1-2): 38-44, 2017.
Article in English | MEDLINE | ID: mdl-27978516

ABSTRACT

BACKGROUND: The public health burden of cancer and dementia in the geriatric population is well documented. There is limited data on how dementia predicts mortality among geriatric patients with solid tumors. The objective of this study is to determine the prognostic significance of dementia on survival in patients with solid tumors. METHODS: We performed a 5-year retrospective study on elderly subjects aged ≥60 years with and without dementia that were diagnosed with solid tumors. RESULTS: Among 3,460 patients with solid tumors, 132 (3.8%) patients were found to have dementia. The median age at diagnosis was 71 years. Kaplan-Meier curves demonstrated that patients with dementia had an inferior median survival compared to the nondemented group (30 vs. 56 months; log-rank p < 0.001). Cox proportional hazard regression modeling identified age >80 years, female gender, diabetes mellitus, congestive heart failure, atrial fibrillation, chronic obstructive pulmonary disease, chronic kidney disease, dementia, and radiation therapy as risk factors for decreased overall survival. CONCLUSIONS: We demonstrated that dementia is associated with shorter overall survival in elderly patients with solid tumors.


Subject(s)
Dementia/mortality , Neoplasms/mortality , Aged , Aged, 80 and over , Comorbidity , Dementia/complications , Diagnostic and Statistical Manual of Mental Disorders , Disease Progression , Female , Humans , Kaplan-Meier Estimate , Male , Middle Aged , Neoplasms/complications , Prognosis , Retrospective Studies , Risk Factors , Sex Factors , Survival Analysis
12.
Cancer Manag Res ; 8: 77-82, 2016.
Article in English | MEDLINE | ID: mdl-27382332

ABSTRACT

Chemotherapy-induced nausea and vomiting (CINV) is a debilitating side effect of antineoplastic agents. Several treatment regimens are used to address this problem. Fosaprepitant is a neurokinin-1 receptor blocker used in the prevention and treatment of CINV, especially for moderately and severely emetogenic chemotherapy. It is highly effective in the treatment of delayed CINV. Data from previous studies show that fosaprepitant is noninferior to aprepitant in the management of CINV. Fosaprepitant is given as a single-dose intravenous infusion, thus offering better patient compliance. The dose-limiting side effect of fosaprepitant is an infusion-related reaction, ranging from pain at the infusion site to thrombophlebitis. This side effect has been reported with coadministration of anthracycline agents.

13.
Oxf Med Case Reports ; 2016(7): 144-6, 2016 Jul.
Article in English | MEDLINE | ID: mdl-27471597

ABSTRACT

Sodium glucose co-transporter (SGLT-2) inhibitor is a relatively new medication used to treat diabetes. At present, the Food and Drug Administration (FDA) has only approved three medications (canagliflozin, dapagliflozin and empagliflozin) in this drug class for the management of Type 2 diabetes. In May 2015, the FDA issued a warning of ketoacidosis with use of this drug class. Risk factors for the development of ketoacidosis among patients who take SGLT-2 inhibitors include decrease carbohydrate intake/starvation, acute illness and decrease in insulin dose. When identified, immediate cessation of the medication and administration of glucose must be done, and in some instances, starting an insulin drip might be necessary. We present a case of a patient with diabetes mellitus being on empagliflozin (SGLT-2 antagonist) who was admitted for acute cholecystitis. The hospital course was complicated by euglycemic diabetic ketoacidosis after being kept nothing per orem before a contemplated cholecystectomy.

14.
J Clin Lab Anal ; 30(6): 1208-1213, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27239981

ABSTRACT

OBJECT: Neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) are simple, inexpensive prognostic markers for various conditions. The objective of this study was to determine the prognostic significance of NLR and PLR in patients with multiple myeloma (MM) in terms of survival. METHOD: A retrospective chart review study was conducted for 175 patients who met the criterion of diagnosis for MM between January 2004 and September 2014. RESULT: The median age of diagnosis was 69 years. Patients were divided into high and low NLR and PLR groups according to cutoff points from the receiver operating characteristic curve (2.78 and 155.58, respectively). The high NLR and PLR groups were associated with lower albumin level and higher staging. The high NLR group experienced inferior median survival compared with the low NLR group (37 vs. 66 months; log-rank P-value 0.005). However, there was no significant difference in median survival between the high and low PLR groups (45 vs. 62 months; P = 0.077). Multivariate analysis demonstrated that NLR is an independent predictor for OS of MM (HR 2.892; P = 0.009). CONCLUSION: We conclude that NLR is an independent prognostic factor for OS in MM.


Subject(s)
Blood Platelets/pathology , Lymphocytes/pathology , Multiple Myeloma/diagnosis , Neutrophils/pathology , Adult , Aged , Aged, 80 and over , Antinematodal Agents , Antineoplastic Agents/therapeutic use , Female , Glomerular Filtration Rate , Humans , Male , Middle Aged , Multiple Myeloma/drug therapy , Prognosis , ROC Curve , Retrospective Studies , Statistics, Nonparametric
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