Case of a 16‐Year‐Old Boy With Headache, Vomiting, and Behavioral Changes

interACTN Case #46: Available: https://interactn.org/2025/04/02/case-46-the-case-of-a-16-year-old-boy-with-headaches-vomiting-and-behavioral-changes/ A 16-year-old boy without any known medical history presented with headaches, vomiting, and behavioral changes. He was in his usual state of health 3 months before admission until the symptoms initially started as headaches and nausea. The headaches got worse when he lay down. The headaches kept worsening but were still manageable with NSAIDs until 1 month before admission. He began vomiting when the headaches were severe. He also felt stiff in his neck. His family noticed that he became irritable. They also noticed that he had irrelevant or incomprehensible talk sometimes. On neurological examination, the patient was alert and well-oriented with intermittent behavioral changes in the form of agitation. His speech was clear but sometimes irrelevant. Reflexes were decreased (1+) but symmetric in the upper and lower extremities. Meningeal irritation signs were revealed. Brain and spine MRI showed hyperintensities along sulcal spaces and the surface of the spinal cord on unenhanced T1-weighted images with diffuse leptomeningeal enhancement involving the entire neuraxis on post-contrast enhanced images (Figure 1). Cerebrospinal fluid (CSF) analysis demonstrated mild pleocytosis (20 cells/mm3, all lymphocytes) with elevated protein (3.77 g/L). CSF cytopathology revealed malignant cells containing melanin pigment, staining positively for melanocyte-specific markers, including HMB-45, Mart-1, and S-100 on immunocytochemistry (Figure 2). Ocular and dermatological examination and whole-body PET found no evidence of nevi or melanoma in other body parts. Primary diffuse leptomeningeal melanomatosis (PDLM). Kundian Guo and Zhen Hong designed the case report, collected data, and consented the patient for participation. Kundian Guo drafted the manuscript. Zhen Hong revised the manuscript. The authors declare no conflicts of interest. The de-identified data that support the findings of this study are available from the corresponding author upon reasonable request and in accordance with current legislation regarding the protection of personal data.

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Journal
Annals of Clinical and Translational Neurology
Published
2025-05-07
DOI
https://doi.org/10.1002/acn3.70052
Primary Topic
Diagnosis and treatment of tuberculosis
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article
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article

Case of a 16‐Year‐Old Boy With Headache, Vomiting, and Behavioral Changes

Kundian Guo, Zhen Hong
Annals of Clinical and Translational Neurology
Diagnosis and treatment of tuberculosis
article

Case of a 16‐Year‐Old Boy With Headache, Vomiting, and Behavioral Changes

Kundian Guo, Zhen Hong
article en

Abstract

interACTN Case #46: Available: https://interactn.org/2025/04/02/case-46-the-case-of-a-16-year-old-boy-with-headaches-vomiting-and-behavioral-changes/ A 16-year-old boy without any known medical history presented with headaches, vomiting, and behavioral changes. He was in his usual state of health 3 months before admission until the symptoms initially started as headaches and nausea. The headaches got worse when he lay down. The headaches kept worsening but were still manageable with NSAIDs until 1 month before admission. He began vomiting when the headaches were severe. He also felt stiff in his neck. His family noticed that he became irritable. They also noticed that he had irrelevant or incomprehensible talk sometimes. On neurological examination, the patient was alert and well-oriented with intermittent behavioral changes in the form of agitation. His speech was clear but sometimes irrelevant. Reflexes were decreased (1+) but symmetric in the upper and lower extremities. Meningeal irritation signs were revealed. Brain and spine MRI showed hyperintensities along sulcal spaces and the surface of the spinal cord on unenhanced T1-weighted images with diffuse leptomeningeal enhancement involving the entire neuraxis on post-contrast enhanced images (Figure 1). Cerebrospinal fluid (CSF) analysis demonstrated mild pleocytosis (20 cells/mm3, all lymphocytes) with elevated protein (3.77 g/L). CSF cytopathology revealed malignant cells containing melanin pigment, staining positively for melanocyte-specific markers, including HMB-45, Mart-1, and S-100 on immunocytochemistry (Figure 2). Ocular and dermatological examination and whole-body PET found no evidence of nevi or melanoma in other body parts. Primary diffuse leptomeningeal melanomatosis (PDLM). Kundian Guo and Zhen Hong designed the case report, collected data, and consented the patient for participation. Kundian Guo drafted the manuscript. Zhen Hong revised the manuscript. The authors declare no conflicts of interest. The de-identified data that support the findings of this study are available from the corresponding author upon reasonable request and in accordance with current legislation regarding the protection of personal data.

Annals of Clinical and Translational NeurologyVol. 12(7)
Sichuan University (CN), West China Hospital of Sichuan University (CN), Shanghai Center for Brain Science and Brain-Inspired Technology (CN), Second Affiliated Hospital of Chengdu University of Traditional Chinese (CN)
Zero hunger
Openalex Percentile: Top 83%
Diagnosis and treatment of tuberculosis
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