Emma L Wetmore, Robert Haddon, Carrie E Robertson, Clayton T Cowl, Wiaam Y Elkhatib, Ivan Garza
{"title":"直升机飞行员头痛、脑脊液淋巴细胞增多伴神经功能缺损。","authors":"Emma L Wetmore, Robert Haddon, Carrie E Robertson, Clayton T Cowl, Wiaam Y Elkhatib, Ivan Garza","doi":"10.3357/AMHP.6702.2025","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The syndrome of transient headache and neurological deficits with cerebrospinal fluid lymphocytosis (HaNDL syndrome) consists of migraine-like headache episodes with >4 h of hemiparesthesia, dysphasia, and/or hemiparesis plus cerebrospinal fluid lymphocytic pleocytosis. While the rarity of HaNDL syndrome often precludes reassurance of the nature of this syndrome, it has consistently been identified as a benign condition that lasts no longer than 3 mo.</p><p><strong>Case report: </strong>In the first week of a viral illness, a 29-yr-old male helicopter pilot experienced acute-onset \"stumbling\" when walking, \"nonsensical speech,\" migraine-like headache, scintillating scotomata, and paresthesias of the tongue and bilateral extremities that lasted for 4-6 h. Work-up included lumbar puncture, revealing lymphocytic pleocytosis. A week later, he experienced word-finding difficulty, right-sided numbness/paresthesia, and severe occipital headache lasting 3 h. A third episode with sensory symptoms involving the tongue and right arm and leg occurred for a few hours 25 d after the onset of the first episode. Symptoms resolved spontaneously. A month following initial discharge, he denied symptom recurrence. Repeat lumbar puncture 4 mo later showed resolution of his pleocytosis. He was considered neurologically recovered 3 mo after symptom onset.</p><p><strong>Discussion: </strong>This patient's transient episodes were consistent with HaNDL syndrome. His symptom resolution involving three episodes within 25 d reflects the transient nature of this condition. It is critical to recognize HaNDL syndrome as a benign, monophasic disorder that resolves within a maximum of 3 mo so that future pilots with a recent history of HaNDL syndrome may safely and expeditiously return to work. Wetmore EL, Haddon R, Robertson CE, Cowl CT, Elkhatib WY, Garza I. Headache and neurological deficits with cerebrospinal fluid lymphocytosis in a helicopter pilot. Aerosp Med Hum Perform. 2025; 96(10):936-939.</p>","PeriodicalId":7463,"journal":{"name":"Aerospace medicine and human performance","volume":"96 10","pages":"936-939"},"PeriodicalIF":0.9000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Headache and Neurological Deficits with Cerebrospinal Fluid Lymphocytosis in a Helicopter Pilot.\",\"authors\":\"Emma L Wetmore, Robert Haddon, Carrie E Robertson, Clayton T Cowl, Wiaam Y Elkhatib, Ivan Garza\",\"doi\":\"10.3357/AMHP.6702.2025\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>The syndrome of transient headache and neurological deficits with cerebrospinal fluid lymphocytosis (HaNDL syndrome) consists of migraine-like headache episodes with >4 h of hemiparesthesia, dysphasia, and/or hemiparesis plus cerebrospinal fluid lymphocytic pleocytosis. While the rarity of HaNDL syndrome often precludes reassurance of the nature of this syndrome, it has consistently been identified as a benign condition that lasts no longer than 3 mo.</p><p><strong>Case report: </strong>In the first week of a viral illness, a 29-yr-old male helicopter pilot experienced acute-onset \\\"stumbling\\\" when walking, \\\"nonsensical speech,\\\" migraine-like headache, scintillating scotomata, and paresthesias of the tongue and bilateral extremities that lasted for 4-6 h. Work-up included lumbar puncture, revealing lymphocytic pleocytosis. A week later, he experienced word-finding difficulty, right-sided numbness/paresthesia, and severe occipital headache lasting 3 h. A third episode with sensory symptoms involving the tongue and right arm and leg occurred for a few hours 25 d after the onset of the first episode. Symptoms resolved spontaneously. A month following initial discharge, he denied symptom recurrence. Repeat lumbar puncture 4 mo later showed resolution of his pleocytosis. He was considered neurologically recovered 3 mo after symptom onset.</p><p><strong>Discussion: </strong>This patient's transient episodes were consistent with HaNDL syndrome. His symptom resolution involving three episodes within 25 d reflects the transient nature of this condition. It is critical to recognize HaNDL syndrome as a benign, monophasic disorder that resolves within a maximum of 3 mo so that future pilots with a recent history of HaNDL syndrome may safely and expeditiously return to work. Wetmore EL, Haddon R, Robertson CE, Cowl CT, Elkhatib WY, Garza I. Headache and neurological deficits with cerebrospinal fluid lymphocytosis in a helicopter pilot. 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Headache and Neurological Deficits with Cerebrospinal Fluid Lymphocytosis in a Helicopter Pilot.
Background: The syndrome of transient headache and neurological deficits with cerebrospinal fluid lymphocytosis (HaNDL syndrome) consists of migraine-like headache episodes with >4 h of hemiparesthesia, dysphasia, and/or hemiparesis plus cerebrospinal fluid lymphocytic pleocytosis. While the rarity of HaNDL syndrome often precludes reassurance of the nature of this syndrome, it has consistently been identified as a benign condition that lasts no longer than 3 mo.
Case report: In the first week of a viral illness, a 29-yr-old male helicopter pilot experienced acute-onset "stumbling" when walking, "nonsensical speech," migraine-like headache, scintillating scotomata, and paresthesias of the tongue and bilateral extremities that lasted for 4-6 h. Work-up included lumbar puncture, revealing lymphocytic pleocytosis. A week later, he experienced word-finding difficulty, right-sided numbness/paresthesia, and severe occipital headache lasting 3 h. A third episode with sensory symptoms involving the tongue and right arm and leg occurred for a few hours 25 d after the onset of the first episode. Symptoms resolved spontaneously. A month following initial discharge, he denied symptom recurrence. Repeat lumbar puncture 4 mo later showed resolution of his pleocytosis. He was considered neurologically recovered 3 mo after symptom onset.
Discussion: This patient's transient episodes were consistent with HaNDL syndrome. His symptom resolution involving three episodes within 25 d reflects the transient nature of this condition. It is critical to recognize HaNDL syndrome as a benign, monophasic disorder that resolves within a maximum of 3 mo so that future pilots with a recent history of HaNDL syndrome may safely and expeditiously return to work. Wetmore EL, Haddon R, Robertson CE, Cowl CT, Elkhatib WY, Garza I. Headache and neurological deficits with cerebrospinal fluid lymphocytosis in a helicopter pilot. Aerosp Med Hum Perform. 2025; 96(10):936-939.
期刊介绍:
The peer-reviewed monthly journal, Aerospace Medicine and Human Performance (AMHP), formerly Aviation, Space, and Environmental Medicine, provides contact with physicians, life scientists, bioengineers, and medical specialists working in both basic medical research and in its clinical applications. It is the most used and cited journal in its field. It is distributed to more than 80 nations.