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Displaying 311 - 320 of 7611 in ACP Online
Noteworthy Resources
Chapter Collaborations (ACP LeaderNet Access Required) This resource is to assist you in working with your chapter's leadership to reflect on where your chapter is, where it would like to elevate to, and how a strategic collaboration could help you achieve that vision.
In the News
Addressing Patient Bias Toward Health Care Workers: Recommendations for Medical CentersBy Kimani Paul-Emile, JD, PhD; Jeffrey M. Critchfield, MD; Margaret Wheeler, MS, MD; Shalila de Bourmont, BS; and Alicia Fernandez, MDThis article offers guidance to organizations on devising effective policies that meet the needs of medical centers, patients, and health care workers across services and roles, including physicians, nurses, and trainees.
From the Trenches
Congratulations! ACP Award for Outstanding Contributions to Improving Well-being and Professional Fulfillment in Internal Medicine Mukta Panda, MD, MACP Chattanooga, Tennessee WBC Emeritus
ACP Multimedia Education
Well-being Champion Training: Data This module explains gathering and analyzing well-being data, followed by discussion and example interventions you can consider. View Here (Must be logged in to ACP Online to access.)
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Patients Before Paperwork
Advocacy in Action ACP Updates Its Climate Change and Health Toolkit The American College of Physicians is renewing its call to members to help mitigate the effects of climate change and educate others on how to do the same. Click below to download the toolkit. View here!
Noteworthy Resources for Well-being
ACP: Design Your Own Well-being Program Explore these tools to create a well-being program tailored to any organization's needs and budget. View here!
In the News
Biden-Harris Administration Announces Nearly $100 Million to Grow the Health Workforce U.S. Department of Health and Human Services: September 17, 2024
From the Trenches
Learn the Importance of Sharing Stories of Vulnerability to Shift the Culture in Medicine: “Stories and Statistics” Annals of Internal Medicine: by Marya J. Cohen, MD, MPH Read about how Dr. Cohen's personal story helped her understand the impact of using stories over numbers to convey meaning behind medicine. Read here! “What Do I Need Today?” With Kerri Palamara, MD, MACP
Displaying 311 - 320 of 6848 in Annals of Internal Medicine
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Displaying 311 - 320 of 3144 in IM Matters
Displaying 311 - 320 of 2393 in ACP Hospitalist
Displaying 311 - 320 of 500 in Annals of Internal Medicine: Clinical Cases
Systemic Immunoglobulin Light Chain Amyloidosis Presenting as Painful Penile Ulcers | Annals of Internal Medicine: Clinical Cases
Immunoglobulin light chain (AL) amyloidosis is a systemic form of amyloidosis that commonly affects the heart, kidney, liver, and nervous system. Penile involvement in AL amyloidosis is rare and thus often not considered in the differential diagnosis for penile ulcers. We report a case of an elderly man with nonhealing, painful penile ulcers who had AL amyloidosis with cardiac, renal, and liver involvement. His penile lesions were successfully treated with surgical resection of the amyloid deposits. Even after serologic relapse of his systemic amyloidosis, he has not had recurrence of his penile ulcers many years later.
Hypoglossal Nerve Palsy Due to a Sublingual Space Abscess | Annals of Internal Medicine: Clinical Cases
We report an unusual case of a hypoglossal nerve palsy secondary to a sublingual space abscess in a previously fit and healthy 59-year-old man. The patient presented with fever, dysphagia, trismus, and a left-sided tongue and floor-of-mouth swelling with left hypoglossal nerve palsy. Computed tomography (CT) scan revealed a 3.5-cm abscess of the left sublingual space. The abscess drained spontaneously while awaiting surgery with resolution of symptoms. Urgent investigation with CT is recommended for every deep neck space infection. Hypoglossal nerve palsy is a rare sign that warrants further investigation to exclude malignancy.
A Young Man With Recurrent Syncope | Annals of Internal Medicine: Clinical Cases
A 35-year-old man presented with recurrent syncope. On examination, wooly hair and palmoplantar hyperkeratosis were seen. Cardiac magnetic resonance imaging showed late gadolinium enhancement, and a genetic test ultimately confirmed the diagnosis of Carvajal syndrome.
Purple Urine Bag Syndrome: “Treated” and Untreated | Annals of Internal Medicine: Clinical Cases
An elderly man with chronic constipation presented with purple urine.
Prostate Adenocarcinoma With Atypical Immunohistochemistry Presenting With a Cheerio Sign | Annals of Internal Medicine: Clinical Cases
The most common cancer in men is prostate cancer. The Cheerio sign is the computed tomography finding of multiple pulmonary nodules with central lucency resembling the ring-shaped Cheerio breakfast cereal. Unlike bone metastasis, pulmonary involvement is less common. The Cheerio sign has malignant and benign etiologies. Thyroid transcription factor-1 (TTF-1) stain is commonly used in the diagnosis of primary lung cancer. TTF-1 positivity in cancers of prostate origin is rare, with only case reports and small case series available in the literature. Metastatic prostate cancer presenting with a Cheerio sign has not been reported in the literature.
“Trench Foot” on the Banks of Lake Geneva: A Severe Case of Nonfreezing Cold Injury | Annals of Internal Medicine: Clinical Cases
Formerly known as “trench foot” or “immersion foot,” nonfreezing cold injury (NFCI) is a rare condition mainly seen among vulnerable groups. We report the case of a homeless male diagnosed with NFCI after having spent 2 days in rainy, cold weather. He presented with white, wrinkled feet and sensorimotor loss. Imaging revealed thrombosis of the leg arteries. No revascularization procedure was possible, and the patient developed soft tissue necrosis requiring bilateral transtibial amputation. Our case highlights the high morbidity linked with NFCI and the need for early recognition and treatment by medical health professionals along with the implementation of preventive measures.
Management of Acute Episodes of Clarkson Disease (Monoclonal Gammopathy-Associated Systemic Capillary Leak Syndrome) With Intravenous Immunoglobulins | Annals of Internal Medicine: Clinical Cases
Monoclonal gammopathy-associated idiopathic systemic capillary leak syndrome (ISCLS, Clarkson disease) is a rare disorder defined by transient but recurrent bouts of hypotensive shock and anasarca resulting from plasma extravasation. Although prophylactic treatment with high-dose intravenous immunoglobulins (IVIG, 1–2 g/kg/mo) prevents most disease flares, its utility for acute episodes of ISCLS is unclear. Here, we report the results of a retrospective study of subjects with acute ISCLS treated at or near the onset of symptoms with IVIG. We found that administration of IVIG with minimal additional intravenous fluids was safe and associated with rapid clinical improvement. IVIG given close to the onset of ISCLS-related symptoms is associated with a favorable outcome.
Fecal Transplant Sustained Colitis Remission on Immunotherapy Resumption | Annals of Internal Medicine: Clinical Cases
Immune checkpoint inhibitors are increasingly used to treat various cancers, but they can cause immune-related adverse events that lead to treatment cessation. Here we report 2 cases of immune-mediated colitis that were treated with fecal microbiota transplant. Both cases had sustained colitis remission, which allowed resumption of immunotherapy.
A Rare Case of Paraneoplastic Dermatomyositis in a Patient With Metastatic Endometrial Cancer | Annals of Internal Medicine: Clinical Cases
Dermatomyositis (DM) is a rare autoimmune myopathy that presents with muscle weakness and characteristic skin manifestations. Certain malignancies are associated with DM, such as stomach, colorectal, ovarian, lung, pancreatic, and non-Hodgkin lymphoma. However, there are only rare reports of endometrial cancer with DM. In this report, we describe a case of anti–TIF-1-gamma and anti-Mi-2 antibody positive DM in a patient with stage IV endometrial cancer. This case illustrates the importance of considering DM as a paraneoplastic syndrome regardless of both stage and type of malignancy.
Giant Cell Tumor in Axial Skeleton With Neurologic Symptoms | Annals of Internal Medicine: Clinical Cases
A healthy 34-year-old man exhibited progressive lower-extremity numbness and weakness. Computed tomography revealed a mass compressing the thoracic spine with associated pathologic fracture. Biopsy showed findings compatible with giant cell tumor of the bone, and H3F3A gene mutation testing confirmed the diagnosis present in the axial skeleton. He was successfully managed with T3–T7 fusion, T5 corpectomy, and physical therapy. This case highlights an atypical presentation of an uncommon neoplasm with associated neurologic deficits.