Yukihiro Goto

Strategies to prevent positioning-related complications associated with the lateral suboccipital approach.

The lateral positioning used for the lateral suboccipital surgical approach is associated with various pathophysiologic complications. Strategies to avoid complications including an excessive load on the cervical vertebra and countermeasures against pressure ulcer development are needed. We retrospectively investigated positioning-related complications in 71 patients with cerebellopontine angle lesions undergoing surgery in our department between January 2003 and December 2010 using the lateral suboccipital approach. One patient postoperatively developed rhabdomyolysis, and another presented with transient peroneal nerve palsy on the unaffected side. Stage I and II pressure ulcers were noted in 22 and 12 patients, respectively, although neither stage III nor more severe pressure ulcers occurred. No patients experienced cervical vertebra and spinal cord impairments, brachial plexus palsy, or ulnar nerve palsy associated with rotation and flexion of the neck. Strategies to prevent positioning-related complications, associated with lateral positioning for the lateral suboccipital surgical approach, include the following: atraumatic fixation of the neck focusing on jugular venous perfusion and airway pressure, trunk rotation, and sufficient relief of weightbearing and protection of nerves including the peripheral nerves of all four extremities.

Abscess formation within a cerebellar metastasis: Case report and literature review

Highlights • We experienced a patient with a brain abscess within a cerebellar metastasis.• A brain abscess within a brain neoplasm is a small entity, and only five cases harboring an abscess within a metastatic brain tumor have been reported to date.• Surgical procedures for brain abscesses and brain tumors are completely different; however, even today, it is difficult to differentiate a brain abscess from a necrotic brain tumor in advance.• Differentiation between the two is important due to different methods of management; preoperative assumption of the possible coexistence of both types of lesions could lead to a good outcome when we encounter a lesion which has both the imaging characteristics.• The preferred treatment of a case with both an abscess and a brain metastasis is complete surgical removal of the tumor and targeted antibiotic therapy for the abscess. The present case highlights the importance of considering coexisting diseases prior to surgery.

Neurological symptoms in a patient with isolated adrenocorticotropin deficiency: case report and literature review

BackgroundIsolated adrenocorticotropic hormone (ACTH) deficiency is a pituitary disorder characterized by reduction only in the secretion of ACTH. Although the underlying mechanism remains to be elucidated, numbers of cases with this entity have been increasing. We experienced a case presenting with gait disturbance necessitating differential diagnosis from idiopathic normal pressure hydrocephalus (iNPH).Case presentationA 69-year-old female with a complaint of difficulty walking and suspected to have iNPH at a prior hospital was referred to our department. For the prior three years, she had suffered from a progressive gait disturbance. Magnetic resonance imaging (MRI) revealed global ventricular dilatation. The typical features of the gait in iNPH cases were all identifiable. Neuropsychological dementia scale tests showed deterioration. However, the major feature of a disproportionately enlarged subarachnoid-space on MRI was not obvious. The patient developed progressively worsening fatigue during hospitalization. Her symptoms resembled those of hypothalamic-pituitary tumor patients. Serum ACTH and cortisol levels were low. While corticotrophin releasing hormone stress tests showed no response, other stress tests using thyrotropin releasing hormone, luteinizing hormone releasing hormone, and growth hormone releasing hormone yielded normal responses, indicating a diagnosis of isolated ACTH deficiency. We initiated corticosteroid therapy, and her gait disturbance improved promptly.ConclusionIsolated ACTH deficiency may have major significance to the differential diagnosis of iNPH. Early consideration of this entity is anticipated to facilitate making an early diagnosis.

A surgical case of cerebral hemorrhage in a patient with factor XI deficiency.

A 63-year-old man suddenly presented with right hemiplegia and was taken to our hospital. Computed tomography (CT) scan revealed subcortical hemorrhage of the left parietal lobe. He had no medical history except hypertension; thus, it initially appeared to be a typical hypertensive hemorrhage. However, blood analysis showed an abnormally elevated activated partial thromboplastin time. One hour after admission, his Glasgow Coma Scale fell from 14 to 11. We performed an echo-guided stereotaxic removal of the hematoma. He improved immediately and was diagnosed with congenital factor XI (FXI) deficiency a few days after surgery. FXI deficiency, described as hemophilic syndrome C, rarely manifests as spontaneous bleeding, but surgical intervention has been known to manifest as bleeding. This case highlights the importance of evaluation of coagulopathies in patients with intracerebral hemorrhage before surgery, and, in cases wherein blood analysis results suggest coexisting coagulation disorders, less invasive surgical methods would likely lead to good outcomes.

Pros and Cons of Tentative Clipping in Intracranial Aneurysm Surgery: Review of 867 Direct Clippings in Single Institution

OBJECTIVE In direct aneurysm surgery, tentative clipping is frequently applied to facilitate aneurysm dissection. However, no systemic review on the pros and cons of tentative clipping has been conducted. This study aimed to investigate the efficacy and concerns of tentative clipping. METHODS A total of 867 direct clippings in 737 patients were performed to treat intracranial aneurysms between 1994 and 2015. We retrospectively investigated the frequency, purpose, location, and adequacy of tentative clipping. RESULTS Tentative clipping was performed in 149 of the 867 aneurysms that were clipped (17.2%). The purpose of tentative clipping was to dissect an aneurysm in 141 (94.6%), separate the vessels from the surface of a sac in 5 (3.4%), and prevent slipping of the final clip in 3 (2.0%) cases. Further dissection revealed that tentative clipping completely excluded the blood flow into the aneurysm in 126 (84.6%) of the 149 cases and incompletely shut it out in 23 (15.4%) cases. Five (21.7%) of the 23 patients with incomplete clipping had intraoperative aneurysm ruptures subsequently. CONCLUSIONS Tentative clipping facilitates dissection of the aneurysm sac from the surrounding structure but can occasionally lead to intraoperative rupture. Before applying tentative clips, surgeons should prepare for temporary clipping or additional tentative clipping in case of a rupture.

Strictly Limited Orbital Pain as Sentinel Headache of Subarachnoid Hemorrhage

BACKGROUND The headache preceding an intracranial aneurysm rupture is called a sentinel headache (SH), and it is characterized by a sudden, intense, and persistent headache. As subarachnoid hemorrhage (SAH) often develops within several weeks of SH, its rapid diagnosis and treatment can improve the prognosis. CASE DESCRIPTION A 52-year-old woman with migraine in her medical history visited the outpatient clinic due to left orbital pain. There was no neurologic deficit. Although magnetic resonance imaging examination found no SAH, a left internal carotid artery-posterior communicating artery bifurcation aneurysm was detected by magnetic resonance angiography. Ten days after the onset of orbital pain, the patient consulted our hospital for a second opinion. We scheduled an elective clipping because the irregular shape of the aneurysm had a high risk of rupture. On the day before surgery, the aneurysm ruptured and led to SAH. Clipping was performed immediately. The patient was discharged with no neurologic deficit. CONCLUSION Clinicians must take into consideration that unilateral orbital pain, though atypical, may be a symptom of SH.

Unusual Clinical Sequelae of Kawasaki Disease—Symptomatic Extracranial Internal Carotid Stenosis in Young Adult

BACKGROUND Kawasaki disease (KD) is an acute systemic vasculitis that primarily affects the coronary artery, but it does not commonly affect the carotid artery. Cerebral infarction (CI) with internal carotid artery stenosis (ICS) in patients with KD has not been reported until now. We report a patient with CI as a remote-phase complication of KD. CASE PRESENTATION A 32-year-old man presented with impaired consciousness. Magnetic resonance imaging and digital subtraction angiography confirmed CI and ICS. He successfully underwent carotid endarterectomy. The resected plaque had pathologic findings of KD, which suggested that the internal carotid artery suffered from chronic inflammation. CONCLUSION KD in childhood may cause symptomatic ICS as a sequela of a remote phase.

Unusual Presentations of Pediatric Skull Hemangiomas: Report of Two Cases

BACKGROUND Intraosseous hemangioma is a rare bone tumor, accounting for 0.7%-1.0% of all bone tumors. It can occur at any age, but only 9% of cases are younger than 10 years old. Although this tumor is usually slow-growing and clinically silent, we experienced 2 pediatric patients undergoing surgery for skull hemangioma who presented with uncommon clinical manifestations. CASE DECRIPTION Case 1 was a 9-year-old boy who presented with sudden onset of headache and was referred to our hospital. Radiologic images revealed an osteolytic oval lesion in the right parietal bone and acute subdural hemorrhage in the right cerebral hemisphere. The right parietal lesion was removed surgically. The lesion was found to have grown into the dura and to be adherent to the pia matter. The removed lesion was histologically confirmed to be a hemangioma. Case 2 was an 8-year-old girl who was referred to our hospital with an elastic mass that had been slowly enlarging for 7 years. Radiologic images revealed an osteolytic oval lesion in the right parietal bone. Surgical removal was thus planned. The lesion was found to be attached to the dura, and we removed the lesion with the surrounding bone and attached dura. Histologic examination confirmed the lesion to be a hemangioma. CONCLUSIONS Although skull hemangiomas show clinical heterogeneity, surgical removal is usually diagnostic and leads to good patient outcomes. On occasion, however, this tumor causes secondary changes in the dura, such that dural incision and dural plasty should be planned in advance of lesion removal.

Microsurgical Removal of Snagged Stent Retriever During Endovascular Embolectomy for Acute Ischemic Stroke

BACKGROUND Catheter-based endovascular thrombectomy has gained popularity for use in patients with acute large-vessel occlusion; however, various complications have been reported. Herein, we present a unique, serious procedure-related complication. CASE DESCRIPTION A 91-year-old woman with acute middle cerebral artery (MCA) occlusion underwent endovascular thrombectomy with a stent retriever, but the device could not be retrieved from the horizontal segment of MCA during the procedure. Subsequently, she underwent emergency craniotomy. The lodged stent was extracted with microforceps using a counter-stretch of the vessels, so as not to avulse the perforating arteries. The stent device was retrieved uneventfully through a sheath introducer that was inserted through the femoral artery. Postprocedural indocyanine green video angiography showed complete recanalization of the MCA and internal cerebral artery. CONCLUSIONS This is a rare case in which successful open surgery was performed to retrieve a snagged stent retriever, with successful recanalization of the large cerebral artery occlusion.

A Pediatric Case of Solitary Myofibroma

A 5-year-old male was referred to our department for evaluation of a firm elastic mass at the back of his head. Clinical examination revealed no abnormalities but the local area was tender. Further clinical and radiological examinations yielded no pathological findings and no other lesions were detected. The lesion was located in the diploic layer of the left parietal bone. The inner layer of the skull intact but the outer layer showed osteolytic change. The lesion did not adhere to the dura mater. The tumor was completely removed with the surrounding bone. Histological examination revealed a mesenchymal tumor comprised of myoid spindle-shaped cells arranged in whorls between muscle cells and fibroblasts and a vascular component around the spindle cells. The final diagnosis was myofibroma. The patient recovered well after the operation and he was discharged from hospital 10 days after surgery. Clinical and radiological follow-up 6 and 12 months later showed neither recurrence of the primary lesion nor any indications of lesions at other sites. Myofibroma is a benign neoplasm composed of myoid cells with thin-walled blood vessels. This tumor, reported to have a wide range of clinical manifestations, is one of the cranial vault tumors. These tumors occur mainly in children although a few affected infants have been reported. Surgical intervention may contribute significantly to the diagnosis of solitary myofibroma and complete removal achieves good outcomes. Herein, we report a 5-year-old male with solitary myofibroma of the skull, presenting as a firm elastic mass in the left parietal bone.