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Similar Publications

Unilateral Sweating: A Case Study of Localized Unilateral Hyperhidrosis.

J Pharm Bioallied Sci

July 2024

Nanavati Max Super Speciality Hospital, LIC Colony, Suresh Colony, Vile Parle West, Mumbai, Maharashtra, India.

Article Synopsis
  • Localized unilateral hyperhidrosis (LUH) is a rare condition characterized by excessive sweating in one specific area, typically without known causes.
  • A case study focuses on a 32-year-old man who experiences sweating on one side of his body during physical activity.
  • Extensive medical tests confirmed that he doesn't have any serious underlying health issues, contributing valuable information to the few documented instances of LUH in otherwise healthy people.
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Objective: Thoracic neurogenic tumors usually present as benign nerve sheath tumors that can be resected via transthoracic or posterior approaches, depending on the anatomical location. Robot-assisted thoracic surgery (RATS) is increasingly being used for the transthoracic approach, but evidence is very limited. The authors initiated the current study to evaluate the efficacy and safety of RATS for thoracic neurogenic tumors.

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Background: Harlequin syndrome is a rare autonomic condition consisting of unilateral facial flushing and sweating induced by heat, emotion or physical activity. The affected side presents anhidrosis and midline facial pallor due to denervation of the sympathetic fibers.

Case Description: This case describes a patient who reported right-side redness of the face associated with hyperhidrosis during physical activity.

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Background: Compensatory sweating (CS) is a frequent health concern following treatment of palmar hyperhidrosis using video-assisted thoracoscopic sympathectomy (VATS) and can reduce level of patient satisfaction.

Methods: A retrospective cohort study including consecutive patients who underwent VATS for primary palmar hyperhidrosis (HH) over a 5-year period was conducted. Various demographic, clinical, and surgical variables were tested for their correlation to postoperative CS through univariate analyses.

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Eccrine angiomatous hamartoma is an uncommon, benign clinical entity constituting a nodular proliferation of eccrine glands and vascular structures localized to the dermis that typically present as unilateral, flesh-colored, erythematous, or violaceous papules on the extremities. These hamartomas may be associated with pain, hyperhidrosis, joint deformity, or functional impairment depending on the severity of the disease process. We present a case of bilaterally symmetric, asymptomatic eccrine angiomatous hamartomas involving all proximal interphalangeal joints of both hands.

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