Artery of Percheron(AOP)embolization or occlusion is a rare cerebrovascular disease that can lead to bilateral thalamic infarction with or without involvement of the upper midbrain.Due to its clinical rarity,lack of typical signs of cerebral infarction,and the diversity of patient symptoms,AOP occlusion-induced cerebral infarction is often misdiagnosed or overlooked,which delays the treatment.This article reported a case of a patient who presented with impaired consciousness as the primary symptom and was initially diagnosed with acute top-of-the-basilar artery embolism related cerebral infarction and underwent emergency endovascular thrombectomy,while the emergency angiography revealed an AOP occlusion.This article also analyzed the clinical features,diagnostic challenges,and treatment strategies of AOP occlusion in combination with the literature,with the aim of providing a reference for clinicians in the diagnosis and treatment of such cases.

Objective:To investigate the efficacy of the patient and family-centered care (PFCC) model in malignant tumor children with peripherally inserted central catheter (PICC) .Methods:Convenience sampling was used to select 136 malignant tumor children with PICC admitted to the Second Affiliated Hospital of Wenzhou Medical University and their families from May 2023 to May 2024 as study subjects. The subjects were divided into an intervention group and a control group of 68 cases each. Control group implemented routine PICC care, and intervention group carried out care based on PFCC model on the basis of control group. Children's self-management ability, catheter maintenance compliance and family satisfaction with nursing were compared between the two groups.Results:A total of 128 children and their families were finally included, 65 in intervention group and 63 in control group. After intervention, the knowledge, attitude, and practice dimension scores and total scores of self-management ability of children in both groups were higher than those before intervention, and the knowledge, attitude, and practice dimension scores and total scores of intervention group were higher than those of control group, with statistically significant differences (all P<0.05) . The excellent rate of catheter maintenance compliance and the nursing satisfaction of the children's families in intervention group were higher than those in control group after intervention, and the differences were statistically significant (all P<0.05) . Conclusions:The application of the PFCC model to malignant tumor children with PICC can enhance children's self-management ability and catheter maintenance compliance, and improve family satisfaction with nursing.

Artery of Percheron(AOP)embolization or occlusion is a rare cerebrovascular disease that can lead to bilateral thalamic infarction with or without involvement of the upper midbrain.Due to its clinical rarity,lack of typical signs of cerebral infarction,and the diversity of patient symptoms,AOP occlusion-induced cerebral infarction is often misdiagnosed or overlooked,which delays the treatment.This article reported a case of a patient who presented with impaired consciousness as the primary symptom and was initially diagnosed with acute top-of-the-basilar artery embolism related cerebral infarction and underwent emergency endovascular thrombectomy,while the emergency angiography revealed an AOP occlusion.This article also analyzed the clinical features,diagnostic challenges,and treatment strategies of AOP occlusion in combination with the literature,with the aim of providing a reference for clinicians in the diagnosis and treatment of such cases.

Objective:To investigate the efficacy of the patient and family-centered care (PFCC) model in malignant tumor children with peripherally inserted central catheter (PICC) .Methods:Convenience sampling was used to select 136 malignant tumor children with PICC admitted to the Second Affiliated Hospital of Wenzhou Medical University and their families from May 2023 to May 2024 as study subjects. The subjects were divided into an intervention group and a control group of 68 cases each. Control group implemented routine PICC care, and intervention group carried out care based on PFCC model on the basis of control group. Children's self-management ability, catheter maintenance compliance and family satisfaction with nursing were compared between the two groups.Results:A total of 128 children and their families were finally included, 65 in intervention group and 63 in control group. After intervention, the knowledge, attitude, and practice dimension scores and total scores of self-management ability of children in both groups were higher than those before intervention, and the knowledge, attitude, and practice dimension scores and total scores of intervention group were higher than those of control group, with statistically significant differences (all P<0.05) . The excellent rate of catheter maintenance compliance and the nursing satisfaction of the children's families in intervention group were higher than those in control group after intervention, and the differences were statistically significant (all P<0.05) . Conclusions:The application of the PFCC model to malignant tumor children with PICC can enhance children's self-management ability and catheter maintenance compliance, and improve family satisfaction with nursing.

Objective To explore prenatal ultrasonic characteristics of fetal Currarino syndrome(CS)and methods for prenatal diagnosis of CS.Methods Two fetuses with CS confirmed by genetic examination were retrospectively analyzed,while 6 CS fetuses with complete prenatal ultrasonic data in literature were reviewed.Prenatal ultrasonic characteristics of CS fetuses and the method for prenatal diagnosis of CS were discussed.Results Among 8 CS fetuses diagnosed with prenatal ultrasound,4 were female singletons with a clear family history of CS,and MNX1 gene mutation was found in 1 fetus.The other 4 fetuses were 2 pairs of male monochorionic twins,all with MNX1 gene mutation.Among 8 CS fetuses,complete triad(sacral agenesis abnormalities,anorectal malformation and presacral mass)were displayed only in 2 fetuses,while all 8 had sacral agenesis abnormalities and 6(6/8,75.00％)were detected with prenatal ultrasound,6 had low location of conus medullaris and 2(2/6,33.33％)detected with prenatal ultrasound.Conclusion Prenatal ultrasound was the first choice for non-invasive diagnosis of fetal CS.When one of sacral agenesis abnormalities,anorectal malformation and presacral mass was found with prenatal ultrasound,the possibility of CS should be considered,and fetal MRI,genetic examination and prenatal genetic counselling should be recommended if necessary.

Objective:To investigate the effect of using the free medial planar artery flap(MPAF) pedicled by the superficial branch of the medial plantar artery in repair of pulp defect of thumb and finger.Methods:Ten patients with pulp defect of thumb and finger were repaired with MPAF of foot in the Department of Hand Surgery of the Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University from November 2020 to January 2022. There were 3 cases of cutting injury, 2 cases of chainsaw injury, 2 cases of extrusion injury and 3 cases of avulsion injury. Digits injuried: 4 index fingers, 3 thumbs, 2 middle fingers, and 1 ring finger. After admission, Doppler ultrasound was performed to understand the running course of medial plantar artery. Emergency surgeries were performed to repair the pulp defects of thumb and finger with free MPAF, and donor sites were repaired by skin grafting. The area of soft tissue defects was 2.0 cm×2.5 cm-3.0 cm×4.5 cm, and the size of flap was 2.5 cm×3.0 cm-3.5 cm×5.0 cm after debridement. Postoperative effect was assessed over the follow-up at outpatient clinics by same group of surgeons. Functional recovery was evaluated according to the Evaluation Standard of Upper Limb Partial Functional of Hand Surgery of Chinese Medical Association.Results:All 10 free MPAFs pedicled by the superficial branch of medial plantar artery survived. After the transfer, the colour, texture and thickness of the flaps were matched with the digit with pulps realistic appearance. Secondary flap thinning surgery was not required. Two cases had blisters at the distal end of the flap, and healed after fluid extraction and dressing change. All patients had 3 to 18 months of follow-up. The TPD of the flap was 4-7 mm. The skin grafts in the donor sites survived well. At the last follow-up, the upper limb function was evaluated according to the Evaluation Standard of Upper Limb Partial Functional of Hand Surgery of Chinese Medical Association, with the results of 8 cases in excellent and 2 in good.Conclusion:Free MPAF pedicled by the superficial branch of medial plantar artery can repair the pulp defect of thumb and finger with reliable blood supply, excellent texture and good appearance. And there is no damage to the main vessels in the donor site.

A 74-year-old male patient underwent posterior lumbar decompression, fusion, and internal fixation under general anesthesia for lumbar spinal stenosis. Sevoflurane (1.5%), propofol, sufentanil, etomidate, and cisatracurium were used for anesthesia, followed by dexamethasone for allergy prevention, cefuroxime for infection prevention, and hydroxyethyl starch for hemodynamic stabilization. Inhalation of sevoflurane (1.5%) and introvenous pumping of remifentanil 300 μg/h and phenylephrine 0.4 mg/h were given for anesthesia maintenance during the operation. The operation process went smoothly and no anaphylaxis occurred within 4 hours. At the end of the operation, vancomycin powder 1 g was given topically at the surgical site and intravenous injection of flurbiprofen axetil 50 mg was given 15 minutes later. Twenty minutes after the medication, the patient′s pulse oxygen saturation was not detectable and the blood pressure fell to 45/20 mmHg. Severe anaphylaxis was diagnosed. The central vein was immediately switched on, and intravenous injection of epinephrine and norepinephrine and intermittently intravenous injection of norepinephrine were given. Ten minutes later, the pulse oxygen saturation returned to 1.00 and 15 minutes later, the blood pressure became stable. At the same time, 2 000 ml of sodium lactate Ringer′s injection was given. The patient was in stable condition 5 hours later and was transferred out of the operating room. The severe anaphylaxis in this patient was considered to be related to vancomycin and flurbiprofen axetil.

A 74-year-old male patient underwent posterior lumbar decompression, fusion, and internal fixation under general anesthesia for lumbar spinal stenosis. Sevoflurane (1.5%), propofol, sufentanil, etomidate, and cisatracurium were used for anesthesia, followed by dexamethasone for allergy prevention, cefuroxime for infection prevention, and hydroxyethyl starch for hemodynamic stabilization. Inhalation of sevoflurane (1.5%) and introvenous pumping of remifentanil 300 μg/h and phenylephrine 0.4 mg/h were given for anesthesia maintenance during the operation. The operation process went smoothly and no anaphylaxis occurred within 4 hours. At the end of the operation, vancomycin powder 1 g was given topically at the surgical site and intravenous injection of flurbiprofen axetil 50 mg was given 15 minutes later. Twenty minutes after the medication, the patient′s pulse oxygen saturation was not detectable and the blood pressure fell to 45/20 mmHg. Severe anaphylaxis was diagnosed. The central vein was immediately switched on, and intravenous injection of epinephrine and norepinephrine and intermittently intravenous injection of norepinephrine were given. Ten minutes later, the pulse oxygen saturation returned to 1.00 and 15 minutes later, the blood pressure became stable. At the same time, 2 000 ml of sodium lactate Ringer′s injection was given. The patient was in stable condition 5 hours later and was transferred out of the operating room. The severe anaphylaxis in this patient was considered to be related to vancomycin and flurbiprofen axetil.

OBJECTIVETo explore the origin and mechanism of small supernumerary marker chromosomes (sSMC) in order to facilitate genetic counseling.

METHODSChromosome karyotypes of two fetuses and their immediate family members were analyzed by conventional G banding. High-throughput whole genome sequencing was used to determine the origin of sSMCs.

RESULTSFetus 1 was shown to have a karyotype of 47,XY,+mar but with normal FISH and B ultrasound findings. Its father also had a 47,XY,+mar karyotype with normal FISH results and clinical phenotype. High-throughput genome sequencing revealed that fetus 1 and its father were both 46,XY,dup(21)(q11.2;q21.1) with a 6.2 Mb duplication of the long arm of chromosome 21. The fetus was born with normal phenotype and developed well. Its grandmother also had a karyotype of 46,XX,t(15;21)(q13;p13) with normal FISH result and clinical phenotype. The karyotypes of its mother and grandfather were both normal. Analysis of fetus 2 showed a 47,XY,+mar karyotype with normal FISH results. High-throughput genome sequencing suggested a molecular karyotype of 46,XX. The fetus was born with normal phenotype and developed well. The karyotypes of its parents were both normal.

CONCLUSIONConsidering their variable origins, identification of sSMC should combine conventional G banding analyses with high-throughput whole genome sequencing for precise delineation of the chromosomes.

Adult ; Amniotic Fluid ; chemistry ; Chromosome Banding ; Chromosome Disorders ; diagnosis ; embryology ; genetics ; Cytogenetics ; Female ; Fetal Diseases ; diagnosis ; genetics ; Genetic Markers ; Humans ; In Situ Hybridization, Fluorescence ; Infant, Newborn ; Karyotyping ; Male ; Pregnancy ; Prenatal Diagnosis ; Young Adult

BACKGROUND: The neurotoxicity and cardiotoxicity of bupivacaine have been reported frequently. However, the studies on bupivacaine-induced muscle toxicity are few.
OBJECTIVE: To establish and evaluate local intramuscular injection of bupivacaine on the changes in histomorphology and ultrastructure of rat multifidus muscle at various time points.
METHODS: A total of 54 male Sprague-Dawley rats weighing 280-320 g were randomly divided into black group (n=18), model group (n=18) and model control group (n=18). Each group was then equal y subdivided into three subgroups according to time points (4, 7 and 14 days) (n=6). Both sides of multifidus muscle of the rats (L4 and L5) were injected with 0.5% bupivacaine. The morphological and ultrastructural changes of multifidus muscle were observed and analyzed with light microscope and transmission electron microscope at 4, 7 and 14 days after model establishment.
RESULTS AND CONCLUSION: (1) A single intramuscular injection of 0.5% bupivacaine induced muscular damage. (2) Hematoxylin-eosin staining results showed fiber necrosis, inflammatory cel infiltration, and a smal amount of macrophages in local skeletal muscle. (3) Under the transmission electron microscope, the structure of myofibrils was destroyed or disintegrated; kinds of bands and lines were indistinct, disrupted or disappeared; the structure of mitochondria was abnormal, the mitochondrial cristae were reduced or disappeared. In the 7- and 14-day groups, multifidus muscle proliferated and repaired. (4) Ultrastructural change scores in skeletal muscle were significantly higher in the model group than in the blank and model control groups (P < 0.05). Above scores were significantly greater in the 4-day group than in the 7- and 14-day groups (P < 0.05), and higher in the 7-day group than in the 14-day group (P < 0.05). (5) Results suggest that a single intramuscular injection of 0.5% bupivacaine can result in pathological changes of skeletal muscle from morphology and ultrastructure. This method can establish a suitable model of skeletal muscle injury.