Abstract
Spontaneous intracranial hypotension (SIH) linked to the leakage of cerebrospinal fluid typically manifests as positional headaches. The connection between connective tissue disorders and SIH is widely recognized. Nevertheless, instances of SIH related to systemic lupus erythematosus are infrequently reported. We report a 42-year-old female with systemic lupus erythematosus and antiphospholipid syndrome who presented with severe orthostatic headaches. Imaging revealed bilateral subdural hematomas and diffuse pachymeningeal enhancement. Conservative treatment was administered, and the patient showed improvement with resolution of symptoms. It is important to note that not all imaging studies consistently reveal all the characteristic features of SIH. Due to these diagnostic limitations, it is crucial for clinicians to consider a combination of patient history, clinical evaluation and imaging findings meticulously.
Introduction
SIH may occur in SLE patients who present with orthostatic headaches.
Case Presentation
We reported a 42-year-old female with SLE and APS presenting with a severe orthostatic headache. The patient's medical history, current medications, and diagnostic findings, including laboratory results and imaging, are discussed.
Discussion
There is no single definitive test to diagnose IH. It often requires a combination of clinical evaluation, imaging, and other diagnostic procedures, which can be inconclusive. Furthermore, it is important to note that not all imaging studies consistently reveal all the characteristic features of SIH.
Conclusion
Due to these diagnostic limitations, it is crucial for healthcare providers to meticulously consider a combination of clinical evaluation, patient history, and imaging findings when suspecting SIH, especially in the context of a SLE patient presenting with headaches.
Author contributions
Arsh Haj Mohamad Ebrahim Ketabforoush, and Nahid Abbasi Khoshsirat involved in study concept and design. Zahra Ahmadian did acquisition of data. Arsh Haj Mohamad Ebrahim Ketabforoush, Zahra Ahmadian, Ali Hosseinpour, and Nahid Abbasi Khoshsirat drafted the manuscript. Nahid Abbasi Khoshsirat, Arsh Haj Mohamad Ebrahim Ketabforoush, Zahra Ahmadian, and Ali Hosseinpour involved in critical revision of the manuscript for important intellectual content. Nahid Abbasi Khoshsirat, Arsh Haj Mohamad Ebrahim Ketabforoush, Zahra Ahmadian, and Ali Hosseinpour involved in administrative, technical, and material support. Nahid Abbasi Khoshsirat supervised the study.
Financial disclosure
The authors have no financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.
Competing interests disclosure
The authors have no competing interests or relevant affiliations with any organization or entity with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.
Writing disclosure
No writing assistance was utilized in the production of this manuscript.
Ethical conduct of research
The authors state that they have obtained verbal and written informed consent from the patient/patients for the inclusion of their medical and treatment history within this case report.
Acknowledgments
The authors want to thank the Clinical Research Development Unit (CRDU) of Shahid Rajaei Hospital, Alborz University of Medical Sciences, Karaj, Iran, for their support, cooperation, and assistance throughout this study.