Statement Of The Clinical Problem Addressed By The Case: We report an atypical clinical presentation of a rapidly progressive neurologic emergency that required prompt investigation and treatment of impending respiratory failure. We discuss the differential diagnosis, evaluation, emergency management, and treatment options of patients with atypical variants of this disorder.
Brief Description Of Case Presentation: A 56-year-old woman with a history of hypothyroidism, anxiety, and depression presented to the emergency department 3 weeks after an upper respiratory and ear infection with cough, pain with sinus palpation, tingling in her fingers bilaterally and right foot, hives, and an episode of blurry vision on awakening. She was discharged home with antibiotics. That evening, she developed rapidly progressing hoarseness and dysphagia and returned to the emergency department. An initial examination and laryngoscopy revealed complete left vocal cord paralysis, consistent with a left cranial nerve X palsy, which prompted a neurologic evaluation. Her examination progressively worsened over the next day requiring mechanical ventilation and ICU admission.
Summary Of The Key Teaching Point In The Case: New-onset bulbar cranial neuropathies should raise concern for neurologic disorders that can be rapidly progressive and result in respiratory failure. Urgent diagnosis and treatment are warranted.
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http://dx.doi.org/10.1212/WNL.0000000000213363 | DOI Listing |
Neurology
April 2025
Department of Neurology, NYU Grossman School of Medicine, NY.
Statement Of The Clinical Problem Addressed By The Case: We report an atypical clinical presentation of a rapidly progressive neurologic emergency that required prompt investigation and treatment of impending respiratory failure. We discuss the differential diagnosis, evaluation, emergency management, and treatment options of patients with atypical variants of this disorder.
Brief Description Of Case Presentation: A 56-year-old woman with a history of hypothyroidism, anxiety, and depression presented to the emergency department 3 weeks after an upper respiratory and ear infection with cough, pain with sinus palpation, tingling in her fingers bilaterally and right foot, hives, and an episode of blurry vision on awakening.
Front Surg
February 2025
Department of Spine Surgery, China-Japan Union Hospital of Jilin University, Changchun, China.
Background: The occurrence of schwannomas at the level of isthmic spondylolisthesis has not yet been reported. Preoperative identification of the responsible lesion and a rational surgical plan are essential for successful surgery.
Case Presentation: We report the case of a 56-year-old woman who presented with a six-year history of low back pain and a three-year history of radiating pain in the left lower extremity.
Neurol Sci
March 2025
Department of Neurosurgery, Nakamura Memorial Hospital, South 1, West 14, Chuo-ku, Sapporo, Hokkaido, 060-8570, Japan.
Bilateral identical duplications of the middle cerebral artery are extremely rare. We report this anatomical variation in a 56-year-old woman. The anatomical variation was identified using magnetic resonance angiography, which was performed to evaluate cerebrovascular disease.
View Article and Find Full Text PDFClin Nucl Med
March 2025
Department of Radiology and Imaging Sciences.
A 56-year-old woman with sickle cell anemia (SCA) and metastatic neuroendocrine tumor refractory to somatostatin analog received 4 cycles of peptide receptor radionuclide therapy (PRRT) with 177Lu-DOTATATE. The treatment schedule was delayed by multiple episodes of hospitalizations related to underlying SCA. PRRT was well-tolerated with stable renal, hematologic, and liver lab parameters.
View Article and Find Full Text PDFClin Nucl Med
February 2025
Department of Nuclear Medicine, The Fourth Hospital of Hebei Medical University.
A 56-year-old woman underwent surgery for clear cell renal cell carcinoma (ccRCC) 8 years ago. The patient incidentally discovered 2 foci in the body and tail of the pancreas by abdominal ultrasound during follow-up. MRI disclosed lesions with central inhomogeneous enhancement and restricted diffusion.
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