1.Suggestion of Follow-Up Period in Nonfunctioning Pituitary Incidentaloma Based on MRI Characteristics
Hyunchul JUNG ; Seung-Yeob YANG ; Keun-Tae CHO
Brain Tumor Research and Treatment 2024;12(1):40-49
Background:
For patients diagnosed with asymptomatic, non-functional pituitary incidentaloma (PI), periodic follow-up is generally proposed. However, the recommended follow-up period differs among existing guidelines and consensus is lacking. Thus, this study aimed to suggest follow-up periods for PI based on MRI characteristics.
Methods:
Between 2007 and 2023, 245 patients who were diagnosed with PI were retrospec-tively assessed. Their mean clinical and neuroradiological follow-up periods were 74.2 and 27.3 months, respectively. Their baseline clinical and neuroradiological characteristics were analyzed. These 245 patients were divided into two groups: those with PI size progression and those without PI size progression. Additionally, neuroradiological features of each group were analyzed according to presumptive diagnoses of PI.
Results:
PI size increased in 33 of 245 patients. For the remaining 212 patients, PI size de-creased or stayed unchanged. Of the 33 patients with PI size progression, ten underwent surgery.Stalk deviation (p<0.001) and lesion enhancement (p=0.001) were significantly more observed in those with PI size progression than in those without PI size progression. MRI morphological factors were not related to changes in PI size in the presumptive Rathke’s cleft cyst group. In the presumptive pituitary adenoma group, absence of tumor enhancement (p<0.001) and stalk deviation (p<0.001) were significantly associated with tumor reduction and progression, respectively.
Conclusion
Our findings support an additional guideline for patients with asymptomatic non-func-tional PI without stalk deviation and enhancement. For these patients, the clinical and neuroradiological follow-up periods could be reduced.
2.Does the Size of Unilateral Decompressive Craniectomy Impact Clinical Outcomes in Patients with Intracranial Mass Effect after Severe Traumatic Brain Injury?
Jinhwan KOO ; Jeongjun LEE ; Su Hwan LEE ; Jung Hyeon MOON ; Seung-Yeob YANG ; Keun-Tae CHO
Korean Journal of Neurotrauma 2021;17(1):3-14
Objective:
Decompressive craniectomy (DC) is one of the treatment modalities in severe traumatic brain injury (TBI), however, there was a lack of evidence for optimal craniectomy size. The authors aimed to investigate optimal DC size and analyze clinical outcome according to craniectomy size.
Methods:
We retrospectively reviewed the medical data of 87 patients with a space occupying lesion following TBI who underwent unilateral DC. Craniectomy size was measured by anterior-posterior (AP) diameter and surface estimate (SE). Mortality, clinical outcome, and complications were collected and analyzed according to craniectomy size.
Results:
Nineteen patients (21.8%) died and 35 patients (40.2%) had a favorable outcome at last follow-up (a mean duration, 30.3±39.4 months; range, 0.2–132.6 months). Receiver operating curve analyses identified AP diameter more than 12.5 cm (area under the curve [AUC]=0.740; p=0.002) and SE more than 98.0 cm2 (AUC=0.752;p=0.001) as cut-off values for survival, and AP diameter more than 13.4 cm (AUC=0.650; p=0.018) and SE more than 107.3 cm2 (AUC=0.685; p=0.003) for favorable outcome. Large craniectomy resulted in a significantly lower mortality rate and a higher rate of favorable outcome than small craniectomy (p=0.005 and p=0.014, respectively). However, procedure related bleeding occurred more frequently in the large craniectomy group (p=0.044).
Conclusion
Unilateral DC size is associated with clinical outcome of patients with a space occupying lesion following severe TBI. Large craniectomy is needed for survival and favorable outcome.
3.Korean Guidelines for the Pharmacological Treatment of Social Anxiety Disorder: Initial Treatment Strategies
Hyungkun YOON ; Dong Jae OH ; Ho Suk SUH ; Kyoung Uk LEE ; Se Won LIM ; Jun Yeob LEE ; Jong Chul YANG ; Jae Hon LEE ; Juwon HA ; Bun Hee LEE ; Seung Gul KANG ; Ho Kyoung YOON ; Jihyun MOON ; Seung Min BAE ; Youngdo KWON ; Hyun Chung KIM ; Kang Seob OH
Psychiatry Investigation 2018;15(2):147-155
OBJECTIVE: The aim of the present study was to provide clinical consensus and evidence regarding initial treatment strategies for the pharmacological treatment of social anxiety disorder (SAD) in Korea. METHODS: We prepared a questionnaire to derive a consensus from clinicians regarding their preference for the pharmacological treatment of SAD in Korea. Data regarding medication regimens and psychotropic drugs used during initial treatment, the doses used, and the pharmacological treatment duration were obtained. Responses were obtained from 66 SAD experts, and their opinions were classified into three categories (first-line, second-line, third-line) using a chi-square analysis. RESULTS: Clinicians agreed upon first-line regimens for SAD involving monotherapy with selective serotonin reuptake inhibitors (SSRIs) or the serotonin-norepinephrine reuptake inhibitor (SNRI) venlafaxine, or combined therapy using antidepressants with betablockers or benzodiazepines on a standing or as-needed basis. First-line psychotropic drug choices for initial treatment included the following: escitalopram, paroxetine, sertraline, venlafaxine, and propranolol. The medication dosage used by domestic clinicians was found to be comparable with foreign guidelines. Domestic clinicians tended to make treatment decisions in a shorter amount of time and preferred a similar duration of maintenance treatment for SAD when compared with foreign clinicians. CONCLUSION: This study may provide significant information for developing SAD pharmacotherapy guidelines in Korea, especially in the early stage of treatment.
Antidepressive Agents
;
Anxiety Disorders
;
Anxiety
;
Benzodiazepines
;
Citalopram
;
Consensus
;
Drug Therapy
;
Korea
;
Paroxetine
;
Propranolol
;
Psychotropic Drugs
;
Serotonin Uptake Inhibitors
;
Sertraline
;
Venlafaxine Hydrochloride
4.The Effect of Preoperative Antiplatelet Therapy on Hemorrhagic Complications after Decompressive Craniectomy in Patients with Traumatic Brain Injury.
Hokyun HAN ; Eun Jung KOH ; Hyunho CHOI ; Byong Cheol KIM ; Seung Yeob YANG ; Keun Tae CHO
Korean Journal of Neurotrauma 2016;12(2):61-66
OBJECTIVE: Traditionally, it is generally recommended that antiplatelet agent should be discontinued before surgery. However, decompressive craniectomy (DC) in patients with traumatic brain injury (TBI) is performed emergently in most cases. Therefore, DC cannot be delayed to the time when the effect of antiplatelet agent on bleeding tendency dissipates. In this study, we evaluated the effect of preinjury antiplatelet therapy on hemorrhagic complications after emergent DC in patients with TBI. METHODS: We retrospectively investigated patients with TBI who underwent emergent DC between 2006 and 2015. The patients were separated into two groups according to the use of preinjury antiplatelet agent: group 1 (patients taking antiplatelet agent) and group 2 (patients not taking antiplatelet agent). The rate of hemorrhagic complications (postoperative epidural or subdural hemorrhage, newly developed, or progression of preexisting contusion or intracerebral hemorrhage within the field of DC) and the rate of reoperation within 7 days after DC were compared between two groups. RESULTS: During the study period, DC was performed in 90 patients. Of them, 19 patients were taking antiplatelet agent before TBI. The rate of hemorrhagic complications was 52.6% (10/19) in group 1 and 46.5% (33/71) in group 2 (p=0.633). The rate of reoperation was 36.8% (7/19) in group 1 and 36.6% (26/71) in group 2 (p=0.986). No statistical difference was found between two groups. CONCLUSION: Preinjury antiplatelet therapy did not influence the rate of hemorrhagic complications and reoperation after DC. Emergent DC in patients with TBI should not be delayed because of preinjury antiplatelet therapy.
Brain Injuries*
;
Cerebral Hemorrhage
;
Contusions
;
Decompressive Craniectomy*
;
Hematoma, Subdural
;
Hemorrhage
;
Humans
;
Platelet Aggregation Inhibitors
;
Postoperative Hemorrhage
;
Reoperation
;
Retrospective Studies
5.Relationship between Neck Length, Sleep, and Cardiovascular Risk Factors.
Tae Seung HAN ; Mi Kyeong OH ; Su Min KIM ; Hyun Ju YANG ; Bum Soon LEE ; Soon Yeob PARK ; Won Joon LEE
Korean Journal of Family Medicine 2015;36(1):10-21
BACKGROUND: Neck circumference, as a predicator of obesity, is a well-known risk factor for obstructive sleep apnea and cardiovascular diseases. However, little research exists on neck length associated with these factors. This study explored the association of neck length with sleep and cardiovascular risk factors by measuring midline neck length (MNL) and lateral neck length (LNL). METHODS: We examined 240 patients aged 30 to 75 years who visited a health check-up center between January 2012 and July 2012. Patients with depressive disorder or sleep disturbance were excluded from this study. MNL from the upper margin of the hyoid bone to the jugular notch and LNL from the mandibular angle to the mid-portion of the ipsilateral clavicle were measured twice and were adjusted by height to determine their relationship with sleep and cardiovascular disease risk factors. RESULTS: Habitual snorers had shorter LNL height ratios (P = 0.011), MNL height ratios in men (P = 0.062), and MNL height ratios in women (P = 0.052). Those snoring bad enough to annoy others had shorter MNL height ratios in men (P = 0.083) and women (P = 0.035). Men with objective sleep apnea had longer distances from the mandible to the hyoid bone to the mandible (P = 0.057). Men with metabolic syndrome had significantly shorter LNL height ratios (P = 0.021), and women with diabetes, hyperlipidemia, and metabolic syndrome had shorter MNL height ratios (P < 0.05). CONCLUSION: This study shows that a short neck by measuring the MNL is probably associated with snoring. In addition, MNL is related to cardiovascular disease risk factors in women.
Anthropometry
;
Cardiovascular Diseases
;
Clavicle
;
Depressive Disorder
;
Female
;
Humans
;
Hyoid Bone
;
Hyperlipidemias
;
Male
;
Mandible
;
Neck*
;
Obesity
;
Risk Factors*
;
Sleep Apnea Syndromes
;
Sleep Apnea, Obstructive
;
Snoring
6.ERRATUM: Correction for the number of the recruited patients and the participating institutions. Prospective randomized controlled trial (phase III) to comparing laparoscopic distal gastrectomy with open distal gastrectomy for gastric adenocarcinoma (KLAS.
Hyung Ho KIM ; Sang Uk HAN ; Min Chan KIM ; Woo Jin HYUNG ; Wook KIM ; Hyuk Joon LEE ; Seung Wan RYU ; GyuSeok CHO ; Chan Young KIM ; Han Kwang YANG ; Do Joong PARK ; Kyo Young SONG ; Sang Il LEE ; Seong Yeob RYU ; Joo Ho LEE
Annals of Surgical Treatment and Research 2014;87(1):51-52
We found an Fig. 1 error in our published article.
7.Prospective randomized controlled trial (phase III) to comparing laparoscopic distal gastrectomy with open distal gastrectomy for gastric adenocarcinoma (KLASS 01).
Hyung Ho KIM ; Sang Uk HAN ; Min Chan KIM ; Woo Jin HYUNG ; Wook KIM ; Hyuk Joon LEE ; Seung Wan RYU ; Gyu Seok CHO ; Chan Young KIM ; Han Kwang YANG ; Do Joong PARK ; Kyo Young SONG ; Sang Il LEE ; Seong Yeob RYU ; Joo Ho LEE
Journal of the Korean Surgical Society 2013;84(2):123-130
A randomized controlled trial to evaluate the long-term outcomes of laparoscopic distal gastrectomy for gastric cancer is currently ongoing in Korea. Patients with cT1N0M0-cT2aN0M0 (American Joint Committee on Cancer, 6th edition) distal gastric cancer were randomized to receive either laparoscopic or open distal gastrectomy. For surgical quality control, the surgeons participating in this trial had to have performed at least 50 cases each of laparoscopy-assisted distal gastrectomy and open distal gastrectomy and their institutions should have performed more than 80 cases each of both procedures each year. Fifteen surgeons from 12 institutions recruited 1,415 patients. The primary endpoint is overall survival. The secondary endpoints are disease-free survival, morbidity, mortality, quality of life, inflammatory and immune responses, and cost-effectiveness (ClinicalTrials.gov ID: NCT00452751).
Adenocarcinoma
;
Disease-Free Survival
;
Gastrectomy
;
Humans
;
Joints
;
Korea
;
Prospective Studies
;
Quality Control
;
Quality of Life
;
Stomach Neoplasms
8.Clinical outcomes of balloon-occluded retrograde transvenous obliteration for the treatment of gastric variceal hemorrhage in Korean patients with liver cirrhosis: a retrospective multicenter study.
Se Young JANG ; Go Heun KIM ; Soo Young PARK ; Chang Min CHO ; Won Young TAK ; Jeong Han KIM ; Won Hyeok CHOE ; So Young KWON ; Jae Myeong LEE ; Sang Gyune KIM ; Dae Yong KIM ; Young Seok KIM ; Se Ok LEE ; Yang Won MIN ; Joon Hyeok LEE ; Seung Woon PAIK ; Byung Chul YOO ; Jae Wan LIM ; Hong Joo KIM ; Yong Kyun CHO ; Joo Hyun SOHN ; Jae Yoon JEONG ; Yu Hwa LEE ; Tae Yeob KIM ; Young Oh KWEON
Clinical and Molecular Hepatology 2012;18(4):368-374
BACKGROUND/AIMS: This study evaluated the clinical outcomes of balloon-occluded retrograde transvenous obliteration (BRTO) for the treatment of hemorrhage from gastric varices (GV) in Korean patients with liver cirrhosis (LC). METHODS: We retrospectively analyzed data from 183 LC patients who underwent BRTO for GV bleeding in 6 university-based hospitals between January 2001 and December 2010. RESULTS: Of the 183 enrolled patients, 49 patients had Child-Pugh (CP) class A LC, 105 had CP class B, and 30 had CP class C at the time of BRTO. BRTO was successfully performed in 177 patients (96.7%). Procedure-related complications (e.g., pulmonary thromboembolism and renal infarction) occurred in eight patients (4.4%). Among 151 patients who underwent follow-up examinations of GV, 79 patients (52.3%) achieved eradication of GV, and 110 patients (72.8%) exhibited marked shrinkage of the treated GV to grade 0 or I. Meanwhile, new-appearance or aggravation of esophageal varices (EV) occurred in 54 out of 136 patients who underwent follow-up endoscopy (41.2%). During the 36.0+/-29.2 months (mean+/-SD) of follow-up, 39 patients rebled (hemorrhage from GV in 7, EV in 18, nonvariceal origin in 4, and unknown in 10 patients). The estimated 3-year rebleeding-free rate was 74.8%, and multivariate analysis showed that CP class C was associated with rebleeding (odds ratio, 2.404; 95% confidence-interval, 1.013-5.704; P=0.047). CONCLUSIONS: BRTO can be performed safely and effectively for the treatment of GV bleeding. However, aggravation of EV or bleeding from EV is not uncommon after BRTO; thus, periodic endoscopy to follow-up of EV with or without prophylactic treatment might be necessary in LC patients undergoing BRTO.
Adult
;
Aged
;
Asian Continental Ancestry Group
;
*Balloon Occlusion/adverse effects
;
Endoscopy, Gastrointestinal
;
Esophageal and Gastric Varices/*complications
;
Female
;
Follow-Up Studies
;
Gastrointestinal Hemorrhage/etiology/prevention & control/*therapy
;
Humans
;
Liver Cirrhosis/*complications
;
Male
;
Middle Aged
;
Odds Ratio
;
Pulmonary Embolism/etiology
;
Recurrence
;
Republic of Korea
;
Retrospective Studies
;
Severity of Illness Index
;
Treatment Outcome
9.Seizures after Spontaneous Intracerebral Hemorrhage.
Kwang Moo WOO ; Seung Yeob YANG ; Keun Tae CHO
Journal of Korean Neurosurgical Society 2012;52(4):312-319
OBJECTIVE: In patients with spontaneous intracerebral hemorrhage (ICH), the risk factors for seizure and the effect of prophylactic anticonvulsants are not well known. This study aimed to determine the risk factor for seizures and the role for prophylactic anticonvulsants after spontaneous ICH. METHODS: Between 2005 and 2010, 263 consecutive patients with spontaneous ICH were retrospectively assessed with a mean follow-up of 19.5 months using medical records, updated clinical information and, when necessary, direct patient contact. The seizures were classified as early (within 1 week of ICH) or late (more than 1 week after ICH). The outcomes were measured with the Glasgow Outcome Scale at discharge and the modified Rankin Scale (mRS) at both 2 weeks and discharge. RESULTS: Twenty-two patients (8.4%; 9 patients with early seizures and 13 patients with late seizures) developed seizures after spontaneous ICH. Out of 263 patients, prophylactic anticonvulsants were administered in 216 patients. The prophylactic anticonvulsants were not associated with a reduced risk of early (p=0.094) or late seizures (p=0.326). Instead, the factors associated with early seizure were cortical involvement (p<0.001) and younger age (60 years or less) (p=0.046). The risk of late seizure was increased by cortical involvement (p<0.001) and communicating hydrocephalus (p=0.004). The prophylactic anticonvulsants were associated with a worse mRS at 2 weeks (p=0.024) and at last follow-up (p=0.034). CONCLUSION: Cortical involvement may be a factor for provoked seizures. Although the incidence of early seizures tended to decrease in patients prescribed prophylactic anticonvulsants, no statistical difference was found.
Anticonvulsants
;
Cerebral Hemorrhage
;
Follow-Up Studies
;
Glasgow Outcome Scale
;
Humans
;
Hydrocephalus
;
Incidence
;
Medical Records
;
Retrospective Studies
;
Risk Factors
;
Seizures
10.Occipital Neuralgia as the Only Presenting Symptom of Foramen Magnum Meningioma.
Nam Hee KIM ; Seung Yeob YANG ; Joon Bum KOO ; Sang Wuk JEONG
Journal of Clinical Neurology 2009;5(4):198-200
BACKGROUND: Occipital neuralgia (ON) is a condition characterized by a paroxysmal stabbing pain in the area of the greater or lesser occipital nerves; it is usually regarded by clinicians as idiopathic. Some have suggested that ON can be induced by trauma or injury of the occipital nerves or their roots, but tumor has rarely been reported as a cause of ON. CASE REPORT: We report herein a case of foramen magnum meningioma in a 55-year-old woman who presented with ON triggered by head motion as the only symptom without any signs of myelopathy. CONCLUSIONS: This case indicates that it is important to consider the underlying causes of ON. Precise neurologic and radiological evaluations such as cervical spine magnetic resonance imaging are needed.
Female
;
Foramen Magnum
;
Head
;
Humans
;
Magnetic Resonance Imaging
;
Meningioma
;
Middle Aged
;
Neuralgia
;
Spinal Cord Diseases
;
Spine

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