CASE REPORT article

Front. Hum. Neurosci., 02 July 2025

Sec. Brain Health and Clinical Neuroscience

Volume 19 - 2025 | https://doi.org/10.3389/fnhum.2025.1559631

Management of a patient with thalamic-capsular hematoma complicated with perilesional edema: a case report

  • Department of Neurophysiothery, Ravi Nair Physiotherapy College, Datta Meghe Institute of Higher Education and Research, Wardha, India

The patient is a 45-year-old woman who was rehabilitated from perilesional oedema with a right thalamic-capsular hematoma. Functional dependence and left-sided hemiparesis were noted. There was considerable improvement in mobility, strength and independence after providing holistic physiotherapy that consisted of multimodal sensory stimulation, tone management, and functional training. Recovery was further enhanced with cutting-edge treatments, including intermittent theta burst stimulation. Remarkable improvements were evidenced in muscle strength, cognitive orientation, and functional independence measures over the entire course of treatment. The article illustrates how quickly and effectively crucial oriented physical therapy at the right point can help reach the best benefit outcome by using the case scenario of a thalamic patient.

Introduction

Thalamic-capsular hematoma with perilesional edema is a significant medical condition characterized by bleeding within the thalamus and the surrounding internal capsule, often accompanied by oedema (swelling) in the adjacent brain tissue (Renard et al., 2014). Thalamic haemorrhage is one of the most common types of nontraumatic intracerebral haemorrhages, accounting for 10 to 15% of all cases (Ruiz-Sandoval et al., 2019). Cerebral haemorrhage occurs in 18.5% of stroke patients, and thalamic haemorrhage accounts for 26% of all cerebral haemorrhage (Hiraoka et al., 2017). Thalamocapsular hematomas are most commonly caused by chronic hypertension, vascular malformations, and cerebral amyloid angiopathy (Qureshi et al., 2001). Other contributing factors include anticoagulant therapy, coagulopathies, trauma, substance abuse, infections, vasculitis, and haemorrhagic brain tumors. Understanding these aetiologies is crucial for guiding management and improving outcomes (Flaherty et al., 2007).

Depending on which parts of the thalamus and internal capsule are involved, common symptoms of a thalamic-capsular haematoma might vary but typically include weakness. Hemiparesis, or weakness on one side of the body, is common in patients and can affect daily tasks and movement. Sensory disturbances include alterations in touch, pain, temperature, and pressure perception, usually affecting one side of the body, and the absence or abnormality of these feelings. Cognitive deficits, including confusion, memory loss, and issues with judgment or decision-making and reasoning are some of the symptoms. Modifications in behaviour: because the thalamus regulates emotions, depression, agitation, and variations in motivation or interest in activities are common which are due to thalamic involvement (Umphred et al., 2013; Roh et al., 2021; Arboix et al., 2007).

Perilesional oedema (PHE) is recognized as a quantifiable marker of secondary brain injury following intracerebral haemorrhage (ICH). Its presence is correlated with poor outcomes, indicating that the extent of oedema can reflect the severity of brain injury and the potential for recovery (Chung et al., 1996). Research indicates that patients with thalamic strokes who receive timely physiotherapy interventions demonstrate better recovery trajectories compared to those who do not. For instance, a study highlighted that early physical therapy not only aids in improving motor performance but also enhances activities of daily living (ADLs) capabilities (Hiraoka et al., 2017). Moreover, the integration of sensory reeducation techniques can help address the sensory deficits often observed in these patients, further contributing to their rehabilitation success, sensory stimulation technique involves using various modalities (auditory, visual, tactile) to enhance sensory recovery (Chen et al., 2021).

This case report aims to detail the physiotherapy interventions employed in a patient with thalamic-capsular hematoma complicated by perilesional oedema. By documenting the rehabilitation process and outcomes, we hope to contribute to the growing body of evidence supporting the importance of targeted physiotherapy in the recovery from thalamic injuries. The insights gained from this case may offer valuable guidance for clinicians managing similar cases in the future.

Patients’ information

A 45-year-old female patient was alright 12 days back when, while brushing her teeth on 26th November at 8 am, she experienced sudden weakness in the left side of her body; she was taken immediately to a local hospital via auto in Chandrapur, where a plain CT of the brain was taken which suggested of right thalamic-capsular hematoma with perilesional oedema. She was admitted immediately and managed conservatively. Due to financial issues, she was brought to AVBRH on 4th November at 9 am, where she was admitted to neuro ICU immediately. The plain CT of the brain was advised by the neurologist and she was managed conservatively. She also has a medical history of chronic kidney disease and hypertension for 2 years. Neuro physiotherapy reference was given on 5th November 2024. She was catheterized on 6th November. For further rehabilitation, the patient was referred. Following referral to the physiotherapy department to improve patient functional independence and gain functional recovery (timeline as summarised in Table 1).

Table 1
www.frontiersin.org

Table 1. Timeline of events.

Timeline of events

Physical and clinical findings

Before the examination, informed consent was obtained. It was noted that a Ryles tube, Foley catheter, IV line, and hemodialysis catheter (present since December 7th) were in place. A thorough neurological examination was performed. The patient was in an obtunded state and was disoriented to time, place, and person, with affected calculation, memory, and attention, and hemodynamically unstable. Motor examination indicated decreased muscle tone in the left-side upper and lower limbs as per the Tone Grading Scale (TGS) it revealed hypotonia in the left upper and lower limbs, and reflexes were diminished for the left side as shown in Table 2. The patient could not roll over in bed, sit, or stand independently.

Table 2
www.frontiersin.org

Table 2. Presentation of reflexes.

Diagnostic assessment

Figures 1, 2 shows acute intraparenchymal haemorrhage with perilesional edema in the right thalamus and chronic lacunar infarct in pons (see Table 3).

Figure 1

Figure 1. CT brain (plain).

Figure 2

Figure 2. MRI brain.

Table 3
www.frontiersin.org

Table 3. Clinical timeline of events demonstrated using the outcome measures.

Follow-up and outcome measures

Therapeutic intervention

Table 4 shows physiotherapy intervention according to the patient problem list. After obtaining an informed consent from the patient’s family, a goal-oriented physiotherapy protocol was designed for a period of 5 weeks. The therapeutic interventions were performed by the same physiotherapist who assessed the patient. There were no complications in the 5 weeks of intervention. The patient did not receive any other interventions like speech therapy and occupational therapy, but the diet of the patient was given accordingly.

Table 4
www.frontiersin.org

Table 4. Structured physiotherapy management aligned with the patient’s rehabilitation needs.

Discussion

The management of thalamic hematomas requires a comprehensive, multidisciplinary approach, often combining medical treatment and surgical interventions. In recent years, the importance of physiotherapy in the rehabilitation phase has been increasingly emphasized due to its significant role in enhancing functional outcomes and improving patients’ quality of life following injury (Arboix et al., 2007).

The improvement observed in the patient can be attributed to the promotion of neuroplasticity and enhanced cortical reorganization. Transcranial magnetic stimulation, particularly intermittent theta burst stimulation (iTBS), has been shown to modulate cortical excitability and facilitate the restoration of disrupted neural circuits, thereby promoting motor recovery in stroke and hemorrhagic brain injuries (Di Lazzaro et al., 2023). Additionally, multimodal sensory stimulation—engaging multiple senses simultaneously—likely reinforced synaptic connections and helped improve interhemispheric communication, a critical factor in regaining motor and sensory function after thalamic injury (Todhunter-Brown et al., 2014). Rood’s approach, utilizing techniques such as tactile stimulation, joint compression, and muscle tapping, provided proprioceptive input that facilitated normalized muscle tone and voluntary movement, supporting spontaneous functional recovery (Ang et al., 2015).

Intervention methods were carefully selected and applied based on the patient’s presentation. TMS was administered over the ipsilesional motor cortex following established safety protocols to enhance motor cortical excitability (Langhorne et al., 2011; Rossini et al., 2015). Multimodal stimulation involved the integration of visual, auditory, and tactile tasks into physiotherapy sessions to maximize sensory feedback and motor planning. Rood’s techniques were applied by combining quick stretches and brushing to facilitate flaccid muscles, along with sustained pressure to inhibit spasticity when present. Each technique was tailored dynamically according to the patient’s daily responsiveness and fatigue levels.

The involvement of a multidisciplinary team significantly influenced the positive outcomes. Collaboration among physiotherapists, neurologists, rehabilitation physicians, occupational therapists, and speech therapists ensured comprehensive care. The team approach allowed for early detection and management of complications such as spasticity, shoulder subluxation, and cognitive deficits, thereby preventing secondary impairments and promoting holistic recovery (Lefaucheur et al., 2020). Regular interdisciplinary meetings and treatment plan adjustments according to the patient’s progress enhanced therapy efficacy.

Several precautions were essential to ensure patient safety and optimize rehabilitation outcomes. During TMS, strict adherence to established guidelines minimized the risk of seizures or adverse neurological effects (Langhorne et al., 2011). Close monitoring during multimodal stimulation sessions prevented overstimulation, fatigue, and frustration, which could hinder neuroplastic changes. When applying Rood’s techniques, it was crucial to avoid excessive or inappropriate sensory input that could provoke maladaptive responses such as spasticity or autonomic dysregulation. Furthermore, early mobilization strategies were employed carefully to avoid musculoskeletal complications such as contractures or pressure ulcers.

Limitations and future scopes

The study was done on a single case for a short period of time. Future scope should focus on conducting prospective study using a large sample size incorporating this protocol to a large sample.

Conclusion

This case study shows how crucial physical therapy is for a patient’s comeback after a thalamic-capsular bleed made worse by swelling around the injury. The patient saw big improvements in movement, sensation, and overall independence thanks to targeted treatments like functional rehab, muscle building normalizing muscle tone, and sensory work. Advanced methods like intermittent theta burst stimulation (iTBS) helped brain rewiring and functional recovery.

To get the best rehab results, you need personalized physical therapy and teamwork across different medical fields. This case gives doctors valuable lessons for treating similar brain problems and highlights why quick physical therapy is key in managing thalamic bleeds.

Data availability statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.

Ethics statement

Written informed consent was obtained from the individual for the publication of any potentially identifiable images or data included in this article.

Author contributions

RG: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing. AT: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing. SD: Writing – original draft, Writing – review & editing. PL: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing.

Funding

The author(s) declare that no financial support was received for the research and/or publication of this article.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The authors declare that no Gen AI was used in the creation of this manuscript.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Ang, K. K., Guan, C., Phua, K. S., Wang, C., Zhou, L., Tang, K. Y., et al. (2015). Brain-computer interface-based robotic end effector system for wrist and hand rehabilitation: results of a three-armed randomized controlled trial for chronic stroke. Front. Neuroeng. 8:30. doi: 10.3389/fneng.2014.00030

Crossref Full Text | Google Scholar

Arboix, A., Rodríguez-Aguilar, R., Oliveres, M., Comes, E., García-Eroles, L., and Massons, J. (2007). Thalamic haemorrhage vs. internal capsule-basal ganglia haemorrhage: clinical profile and predictors of in-hospital mortality. BMC Neurol. 7:32. doi: 10.1186/1471-2377-7-32

PubMed Abstract | Crossref Full Text | Google Scholar

Chen, Y., Chen, S., Chang, J., Wei, J., Feng, M., and Wang, R. (2021). Perihematomal edema after intracerebral hemorrhage: an update on pathogenesis, risk factors, and therapeutic advances. Front. Immunol. 12:740632. doi: 10.3389/fimmu.2021.740632

PubMed Abstract | Crossref Full Text | Google Scholar

Chung, C. S., Caplan, L. R., Han, W., Pessin, M. S., Lee, K. H., and Kim, J. M. (1996). Thalamic haemorrhage. Brain 119, 1873–1886. doi: 10.1093/brain/119.6.1873

PubMed Abstract | Crossref Full Text | Google Scholar

Di Lazzaro, V., Pilato, F., Dileone, M., Profice, P., Capone, F., Ranieri, F., et al. (2008). Modulating cortical excitability in acute stroke: a repetitive TMS study. Clin Neurophysiol. 119:715–723. doi: 10.1016/j.clinph.2007.11.049

PubMed Abstract | Crossref Full Text | Google Scholar

Flaherty, M. L., Kissela, B., Woo, D., Kleindorfer, D., Alwell, K., Sekar, P., et al. (2007). The increasing incidence of anticoagulant-associated intracerebral hemorrhage. Neurology 68, 116–121. doi: 10.1212/01.wnl.0000250340.05202.8b

PubMed Abstract | Crossref Full Text | Google Scholar

Hiraoka, S., Maeshima, S., Okazaki, H., Hori, H., Tanaka, S., Okamoto, S., et al. (2017). Factors necessary for independent walking in patients with thalamic hemorrhage. BMC Neurol. 17:211. doi: 10.1186/s12883-017-0991-2

PubMed Abstract | Crossref Full Text | Google Scholar

Langhorne, P., Bernhardt, J., and Kwakkel, G. (2011). Stroke rehabilitation. Lancet 377, 1693–1702. doi: 10.1016/S0140-6736(11)60325-5

PubMed Abstract | Crossref Full Text | Google Scholar

Lefaucheur, J. P., Aleman, A., Baeken, C., Benninger, D. H., Brunelin, J., Di Lazzaro, V., et al. (2020). Evidence-based guidelines on the therapeutic use of repetitive transcranial magnetic stimulation (rTMS): an update (2014–2018). Clin. Neurophysiol. 131, 474–528. doi: 10.1016/j.clinph.2019.11.002

PubMed Abstract | Crossref Full Text | Google Scholar

Qureshi, A. I., Tuhrim, S., Broderick, J. P., Batjer, H. H., Hondo, H., and Hanley, D. F. (2001). Spontaneous intracerebral hemorrhage. N. Engl. J. Med. 344, 1450–1460. doi: 10.1056/NEJM200105103441907

PubMed Abstract | Crossref Full Text | Google Scholar

Renard, D., Castelnovo, G., Campello, C., Bouly, S., Le Floch, A., Thouvenot, E., et al. (2014). Thalamic lesions: a radiological review. Behav. Neurol. 2014:154631. doi: 10.1155/2014/154631

PubMed Abstract | Crossref Full Text | Google Scholar

Roh, S., Miyamoto, S., Kitamura, Y., Mito, D., and Okazaki, M. (2021). Secondary vulvar reconstruction using bilateral gluteal fold flaps after radical vulvectomy with direct closure. Plast. Reconstr. Surg. Glob. Open 9:e3550. doi: 10.1097/GOX.0000000000003550

PubMed Abstract | Crossref Full Text | Google Scholar

Rossini, P. M., Burke, D., Chen, R., Cohen, L. G., Daskalakis, Z., Di Iorio, R., et al. (2015). Non-invasive electrical and magnetic stimulation of the brain, spinal cord, roots and peripheral nerves: basic principles and procedures for routine clinical and research application. Clin. Neurophysiol. 126, 1071–1107. doi: 10.1016/j.clinph.2015.02.001

PubMed Abstract | Crossref Full Text | Google Scholar

Ruiz-Sandoval, J. L., Chiquete, E., Parra-Romero, G., Carrillo-Loza, K., Parada-Garza, J. D., Pérez-Gómez, H. R., et al. (2019). Hypertensive thalamic hemorrhage: analysis of short-term outcome. Int. J. Neurosci. 129, 189–194. doi: 10.1080/00207454.2018.1518905

PubMed Abstract | Crossref Full Text | Google Scholar

Todhunter-Brown, A., Baer, G., Campbell, P., Choo, P. L., Forster, A., Morris, J., et al. (2014). Physical rehabilitation approaches for the recovery of function and mobility following stroke. Cochrane Database Syst. Rev. 2023:CD001920. doi: 10.1002/14651858.CD001920.pub3

PubMed Abstract | Crossref Full Text | Google Scholar

Umphred, D. A., Lazaro, R. T., Roller, M. L., and Burton, G. U. (2013). Umphred’s neurological rehabilitation. 6th Edn. St. Louis: Elsevier Mosby.

Google Scholar

Keywords: intermittent theta burst stimulation, thalamic hematoma, perilesional edema, multimodal stimulation, physiotherapy management

Citation: Gandhi R, Tikariha A, Dey S and Ladkhedkar P (2025) Management of a patient with thalamic-capsular hematoma complicated with perilesional edema: a case report. Front. Hum. Neurosci. 19:1559631. doi: 10.3389/fnhum.2025.1559631

Received: 13 January 2025; Accepted: 02 June 2025;
Published: 02 July 2025.

Edited by:

Estêvão Rios Monteiro, University Center Augusto Motta, Brazil

Reviewed by:

Karina Santos Guedes De Sá, State University of Campinas, Brazil
Thaís Horsth, University Center Augusto Motta, Brazil

Copyright © 2025 Gandhi, Tikariha, Dey and Ladkhedkar. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Anshu Tikariha, YW5zaHUudGlrYXJpaGFAZG1paGVyLmVkdS5pbg==

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.