Monday, May 31, 2021

The meniscus sign: An endoscopic finding of cerebrospinal fluid rhinorrhea

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https://bjo.bmj.com/content/bjophthalmol/70/8/570.full.pdf
British Journal of Ophthalmology, 1986, 70, 570-574
Pseudoepiphora from cerebrospinal fluid leak:
case report
ROBERT M DRYDEN,' AND ALLAN E WULC2
From the 'Department of Ophthalmology, University ofArizona, Tucson, Arizona, and
2University of Pennsylvania Scheie Eye Institute, Department of Ophthalmology, Philadelphia,
Pennsylvania, USA
SUMMARY A 4-year-old tearing child with obstruction of the nasolacrimal duct was treated with
dacryocystorhinostomy three years after naso-orbital injury. However, what appeared to be
tearing peristed, and meningitis developed. Coronal CT scans demonstrated traumatic encephalocele of the posterior superior orbital roof. A chronic orbital cerebrospinal fluid (CSF) leak was
diagnosed. To our knowledge no case of chronic CSF leak has been reported that simulated tearing
in an otherwise asymptomatic child. In the tearing patient who has a naso-orbital fracture the
possibility of chronic CSF leak should be considered.
Lacrimal outflow obstruction is a well recognised
complication of midfacial fractures involving the
maxilla, the lacrimal bones, or the ethmoids.18
Common manifestations of obstruction to the
lacrimal outflow system include epiphora, dacryocystitis, or mucocele.
A case of epiphora thought to be secondary to
nasolacnmal duct obstruction following midfacial
trauma is herein described. A 4-year-old child seen
two years after naso-orbital injury had traumatic
lacrimal duct obstruction and underwent uncomplicated dacryocystorhinostomy (DCR).
The aetiology of tearing in this child was chronic
post-traumatic cerebrospinal fluid (CSF) leakage
that occurred simultaneously with lacrimal duct
obstruction. Despite a successful, DCR, chronic
copious CSF leakage simulating tearing continued.
To our knowledge this is the first reported case of
pseudoepiphora caused by chronic CSF leakage in an
otherwise asymptomatic child.
After midfacial fracture chronic CSF leak should
be considered in the differential diagnosis of tearing,
and the appropriate laboratory and radiographic
tests should be performed.
Case report
A 4-year-old boy was seen with epiphora of the right
eye of two years' duration. A motor-car accident two
Correspondence to Robert M Dryden, MD, 601 N Wilmot Road,
Suite 58, Tucson, Arizona 8571 1, USA.
years previously resulted in hospital admission,
where lethargy progressing to coma and blood in the
middle ear led to the diagnosis of basilar skull
fracture. Computerised axial tomography (CT) was
done three times while he was in hospital and the
scans were reported as normal.
Immediately following hospital discharge persistent right-sided tearing was noted. There was no
irrigation or pain, and tearing was not related to
eating or salivation. Ocular examination showed
visual acuities of 20/30 in both eyes. Right inferior
oblique overaction was noted with a V-pattern
exotropia. Palpation of the orbit revealed no anterior
defects and a normally positioned, non-pulsatile
globe with no rim defects.
Lacrimal examination with a Jones primary dye
test showed no passage of dye after 40 minutes.
Traumatic lacrimal drainage obstruction was inferred.
An examination under anaesthesia revealed an
obstructed nasolacrimal duct. No fluid could be
irrigated through either the upper or lower canaliculus into the nose. Probing revealed a tight internal
common punctum and an obstructed nasolacrimal
duct.
A dacryocystorhinostomy with canalicular intubation with silicone tubing was performed. The bone
was thickened, presumably from past naso-orbital
fracture. The patient received 500 mg of intravenous
cephazolin (Kefzol) and oral cephalosporins were
continued for seven days.
570
Pseudoepiphora from cerebrospinalfluid leak: case report
On the fifth postoperative day mild erythema of
the scar site was noted. Tearing had not ceased.
One week after operation the patient developed
fever with headache and vomiting. He was admitted
to a community hospital with a presumptive diagnosis
of periorbital cellulitis and begun on intravenous
cephazolin. Two days later he complained of neck
pain. A lumbar puncture was done which showed
cloudy CSF, raising the possibility of bacterial meningitis. An additional antibiotic was instituted. An axial
CT scan was performed which showed air and soft
tissue swelling of the right orbit consistent with the
operative appearances as well as an opacity of the
right ethmoids consistent with the postoperative
haemorrhage he had had.
In the ensuing two weeks the patient developed
recurrent spiking fevers accompanied by meningeal
signs. Intravenous antibiotics were altered to methicillin and chloramphenicol, and he remained afebrile
until three weeks after operation, at which time
another temperature spike to 101 degrees was noted.
The patient was transferred to Tucson Medical
Center for further evaluation.
On admission, the temperature was 38 3°C and the
vital signs were otherwise normal. No periorbital
cellulitis was noted. The dacryocystorhinostomy scar
was healing well. The silicone stent was in place.
Tearing was persistent and the results of the eye
examination were otherwise normal. The medical
examination, including a neurological examination,
gave results within normal limits. All laboratory tests
including examination of the CSF gave normal
results.
On the second day in hospital an ophthalmic plastic
surgery opinion was sought. The child continued to
Fig. 1 Coronal CTdemonstrating DCR ostium and
thickening ofnasal mucosa on the right (arrow).
'tear' profusely in the right eye. A Jones primary dye
test showed dye in the oropharynx at 2 minutes. It
was concluded that the dacryocystorhinostomy surgery had been successful and that causes of pseudoepiphora should be sought to explain the 'tearing'.
Our examination included a Dextrostix test of the
tear fluid. The sugar content of the tear fluid was
observed. The Dextrostix test of the right eye showed
a glucose level of 100 to 180 mg/dl (5-6-10.0 mmol/l).
The glucose level from the left eye was less than 100
mg/dl (5.6 mmol/l). A specimen of the patient's tears
was collected and sent for laboratory analysis. A
discrepancy of 2 to 1 in the glucose concentration
existed in the right and left eyes. The data strongly
suggested CSF leakage into the orbit. A CT scan was
performed (Figs. 1 and 2). A gas lucency in the region
of the right orbit with thickening of the right medial
rectus and opacification of the right ethmoid was
observed. Anteriorly the DCR ostium was visible
along with thickening of the nasal mucosa (Fig. 1). A
bony defect was noted in the posterior orbit that
did not communicate with the DCR ostium (Fig.
2).
On the tenth day in hospital a frontal craniotomy
was performed. An encephalocele wasfound into a
fracture in the posterior medial orbital roof. It was
retracted from the fracture site, and a Silastic implant
was placed over the defect. The dural tear was noted
and repaired with a free pericranial graft and closed
with a single running suture. Postoperatively the
patient did well and was discharged six days later.
Tearing ceased immediately after surgery. Measured
glucose levels in both eyes were the same and less
than 100 mg/dl (5.6 mmol/l).
'demonstrating defect in orbital roofon
the rignt (arrows).
571
Robert MDryden and Allan E Wulc
Discussion
CSF leak has been reported to occur in 6% to 35% of
patients with severe non-penetrating intracranial
injury.'59 It occurs in approximately 20% of patients
with midfacial fracture or fractures through the
paranasal sinuses.:
CSF leaks are rare in children below the age of 2
because of the flexibility of the cranial base and the
relative immaturity of the paranasal sinuses. However, in children older than 2, CSF leakage is by no
means uncommon."'
Traumatic CSF leaks usually result from tears in
the dura at the skull base that allow CSF to escape
from the subarachnoid space into the nasopharynx,
the paranasal sinuses, or subcutaneously. The floor
of the anterior cranial fossa, particularly the cribriform plate area, is thin, and the dura at this site firmly
invests the olfactory fissure where the olfactory nerve
penetrates the skull. Midfacial trauma may result in
penetration of the anterior cranial fossa by ethmoidal
roof or wall fragments and dural tear. CSF escapes
immediately. If the edges of the dura are in apposition and do not gape, healing is relatively rapid and
CSF leak resolves in three to 10 days. Sinus mucosa
may bridge a gaping dural defect and cause leakage to
cease. However, if bony spicules project through the
tear, a portion of the brain herniates through the
defect. If a large dural defect is present, healing may
be incomplete. High CSF flow due to coughing or
straining may also result in late onset of CSF leakage
due to rupture of a partially healed tear. Dural tears
may be enlarged by brain and high amplitude CSF
pulsation with resultant erosion of bone.9 "
The diagnosis, aetiology, and management of
fractures of the orbital roof have been well described by McClachan et al. 2 Rhinorrhea is the
most common presenting symptom of CSF leakage
and presents in 25% of patients with midfacial
fracture.' Hypo-osmia or anosmia may occur from
damage to olfactory nerve fibres in 5% of patients.9
Smell may be intact in patients who have anteriorly
placed frontal sinus fractures or sphenoidal sinus
fractures. If fracture of the petrous portion of the
temporal bone has occurred, CSF from the middle or
posterior cranial fossa may escape into the mastoids
and produce middle ear fluid mimicking serous otitis
media. Rarely CSF tracks subcutaneously, producing
a subepicranial hydroma.'3 Headache occurs in 15%
of patients with CSF leakage and is therefore thought
to be an inconstant symptom.9 Meningitis occurs in
between 3% and 50% of cases of CSF leakage and the
incidence is higher when the leakage is chronic."`116
The observant patient may describe a gush of salty
fluid, or choke on arising in the morning. In the
recumbent position leaking CSF collects dependently
in the sphenoid sinus. On the patient's standing, an
influx of CSF collected overnight rushes into the
oropharynx causing the so-called reservoir sign.'7
Other signs of CSF leakage include frequent
awakening from sleep with coughing fits and soaking
of the bed sheets with clear nasal discharge each
night. Rhinitis has also been described from chronic
CSF leakage.9"
CSF leakage following midfacial fracture in an
otherwise asymptomatic patient may be confused
with traumatic epiphora. In a series of 300 patients
with midfacial fracture where 35% had CSF leakage,
5 3% had concomitant epiphora or dacryocystitis.5 In
a series of 100 patients reported by Campbell with
midfacial fracture 12% had complaints of tearing.'8
Naso-orbital trauma may injure the medical palpebral tendon, lacerate or compress the nasolacrimal
sac or duct, or cause cicatricial ectropion of the lower
lid or punctal malposition.478 While CSF leakage
usually resolves, dacryocystitis and epiphora commonly persist until surgically treated.
Few cases of chronic CSF leakage into the orbit
have been reported in the neurosurgical or ophthalmic literature. In a review of giant epidermoid
and dermoid tumors of the orbit Carey described two
cases of chronic CSF leakage into the orbit thought to
be from direct communication between the subarachnoid space and the inner portion of the tumour. 9 In
his series other symptoms including pulsating proptosis, and extraocular movement limitation were also
observed. 9
A case of traumatic CSF fistula simulating epiphora
occurred in a child 8 months of age and was reported
in the neurosurgical literature.2" Epiphora occurred
immediately following head trauma. The patient
presented with coma, hemiparesis, and facial weakness and developed a pulsating exophthalmos accompanied by bruit and chronic epiphora. Chemosis and
epiphora resulted from a leak through the ethmoidal
sinuses directly to the conjunctiva. The child underwent surgical repair of the fistula soon afterwards.
A case of CSF fistula in a 22-year-old victim of a
motor vehicle accident with a cranial nerve palsy has
been reported. This patient had a pulsatile right
upper lid and chemosis from direct subarachnoid
communication with the upper lid. No tearing was
observed at any time.2'
The present case of CSF leakage differs from the
above-mentioned cases and has many interesting and
hitherto undescribed features. It occurred chronically and continuously in an awake and alert child for
a period of three years following injury. Proptosis,
chemosis, or eyelid swelling were not noted at any
time, and neurological deficit did not develop. No
pulsations were observed. Finally, tearing was not
suspected to be secondary to orbital CSF leakage
572
Pseudoepiphorafrom cerebrospinalfluid leak: case report
until after successful lacrimal drainage surgery had
been performed.
CSF leakage occurred as a result of dacryocystorhinostomy surgery in two cases reported by Neuhaus
and Baylis and may occur if bone removal extends to
the level of the cribriform plate.22 The same authors
noted an average of 5 mm between the nasal ostium
and the floor of the anterior cranial fossa.22 While it is
possible that in the reported cases DCR surgery
could have created a CSF leak, it is unlikely. Tearing
was chronic prior to surgery and persisted after
surgery, and it promptly resolved following neurosurgical repair of the posterior orbital encephalocele.
Other unlikely hypotheses that might explain the
findings in the presented case include the possibility
that CSF leaked from the canaliculi in retrograde
fashion from the abnormality of the cranial vault,
simulating tearing. The CT evidence for this theory is
lacking, as the encephalocele was well posterior to
the lacrimal drainage system. While remanipulation
of a traumatically altered orbit and cranial base
undoubtedly introduced meningeal infection, the
pathway of CSF leakage from posterior orbit to the
tear film is a matter of speculation.
Reagent strips such as Dextrostix and Labstix
commonly used for urine glucose determination,
while not helpful in distinguishing CSF from nasal
discharge,'223-26 may be helpful in diagnosing CSF
leakage into the orbit. CSF glucose is approximately
70% of that of serum glucose. Normal levels of
glucose in tears are insignificant.26 27 For the purposes
of the clinical examination in the reported case, tear
concentration in 20 normal individuals without diabetes mellitus was measured with a Labstix reagent
strip by placing it directly on the tear meniscus and
waiting until wetting had occurred. After 30 seconds
the glucose level was measured by matching the
colour of the paper with the colour of the glucose as
determined on the table found on the bottle. In all
patients the glucose level was found to be within 0
and 100 mg/dl (0 and 5 6 mmol/l). In the case
described here the glucose level on the uninvolved
side was from 0 to 100 mg/dl, corresponding to the
normal value. On the involved side the tear glucose
level was between 100 and 180 mg/dl (5.6 and 10-0
mmol/l). The higher glucose level on the involved
side in this patient was confirmed by laboratory
analysis. A large sample needs to be collected for
glucose concentration to be analysed in a laboratory.
The reagent strips are inexpensive, immediate, and
require substantially less tear volume and were
effective in diagnosing the leakage.
The site of CSF leakage may be localised radiographically with or without the aid of contrast
material. Skull films may show an air fluid level in the
sinuses.9 Materials can be instilled intrathecally to
demonstrate leakage of CSF. Methylene blue and
fluorescein were at one time injected but have been
abandoned owing to numerous complications."2"29
Radioiodide labelled serum albumin and technetium
are used to directly visualise CSF leak with cisternography and are diagnostic in 86% of cases."'
Metrizamide encephalocistemography with high
resolution CT is mandatory in evaluation of the
patient with a suspected chronic orbital CSF leak. In
our patient CT scans with axial views were obtained
at the time of the original trauma and repeatedly
thereafter to evaluate brain, orbits, and skull base
and were all within normal limits. One week following DCR axial CTs again did not show any abnormality of the skull base or orbital roof. However,
coronal CTs with 1-5 mm cuts clearly show a posterior bony defect and suggested meningoencephalocele and chronic CSF leak. The different perspective
offered by directly formed coronal views may be an
asset in considering the possibility of chronic CSF
leakage into the orbit.
When a CSF leak is noted in the early period post
midfacial injury, opinions are varied as to whether
direct and immediate reduction of facial fracture or
repair of dural tear is indicated. Most authors
recommend bed rest with the head of the bed raised.
Prophylactic antibiotics are administered intravenously. Bed rest, stool softeners, and medication
to prevent coughing or straining are recommended.
A lumbar drain, placed in the lumbar subarachnoid
space, may be useful in lessening CSF flow through
the dural rent, thus allowing repair to take place.
Likewise, acetazolamide may be administered to
decrease the production of CSF.
The majority of CSF leaks heal without the need
for surgery.9" When the neurological condition has
stabilised, fractures may be reduced with the
realisation that additional trauma to the dura may
result.
The treatment of chronic persistent CSF leak is
neurosurgical."I 1617 If meningitis has supervened, an
adequate period of time should elapse for the patient
to be on appropriate antibiotics. Chronic CSF leaks
usually do not subside spontaneously. The area of the
dural rent must be localised and repaired. In the
reported case a frontal craniotomy with exposure of
the fracture site, Silastic roof implant, and epicranial
duroplasty were performed. The techniques of this
neurosurgical procedure go beyond the scope of this
paper.
Patients who tear after naso-orbital trauma must
be suspected of having a CSF leak even if signs of
nasolacrimal duct obstruction are present. It may be
useful to ask patients specifically about rhinorrhoea
or anosmia, as well as to examine for increased
tearing during the Valsalva manoeuvre. CT scans
573
Robert MDryden and Allan E Wulc
should be reviewed if they have been performed and
coronal sections are preferred. Finally, Dextrostix
can be used to obtain an objective measurement of
tear sugar level in order to diagnose chronic orbital
CSF leak. If CSF leak is a possibility, the patient
should be referred for neurosurgical consultation
prior to any lacrimal surgical intervention.
The authors are grateful to Jack H Dunn, the neurosurgeon involved
in this case.
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Acceptedfor publication 3 December 1985.
574

In chest roentgenograms, the pulmonary meniscus sign is a crescent-shaped inclusion of air surrounded by consolidated lung tissue. The common cause is aspergilloma. A hydatid cyst is, however, the most common cause in endemic areas.

Int Forum Allergy Rhinol. 2021 May 31. doi: 10.1002/alr.22830. Online ahead of print.

NO ABSTRACT

PMID:34057288 | DOI:10.1002/alr.22830

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Headache due to Bilateral Subacute Subdural Hematomas following Intracranial Hypotension Caused by Cervical Disc Herniation

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Case Rep Neurol. 2021 Apr 19;13(1):246-250. doi: 10.1159/000511428. eCollection 2021 Jan-Apr.

ABSTRACT

Spontaneous intracranial hypotension (SIH) is caused by spinal leakage of cerebrospinal fluid (CSF) and typically causes orthostatic headache which is relieved by lying in a recumbent position. We describe the case of a 44-year-old male suffering from orthostatic headaches accompanied by symptomatic cervical disc herniation, for which he had an anterior cervical discectomy and fusion (ACDF). Computerized tomography of the brain at the emergency department 1 week after this procedure showed bilateral subacute subdural hematomas. In retrospect, the positional headache had been present for 3 months prior to the ACDF, and magnetic resonance imaging of the cervical spine prior to the ACDF already showed signs of an extradural CSF collection indicating intracranial hypotension. This case highlights the possibility of SIH caused by a spinal dural l eak due to cervical disc herniation.

PMID:34054463 | PMC:PMC8138280 | DOI:10.1159/000511428

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Helicobacter pylori infection over bile reflux: No influence on the severity of endoscopic or premalignant gastric lesion development

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Exp Ther Med. 2021 Jul;22(1):766. doi: 10.3892/etm.2021.10198. Epub 2021 May 14.

ABSTRACT

Helicobacter (H.) pylori infection and duodenogastric reflux (DGR) are both linked to endoscopic and premalignant gastric lesion development, but it is still unclear whether they are independent or have a causal relationship. This study investigated the histologic gastric changes in patients with primary DGR and H. pylori infection, as well as their endoscopic findings, symptoms, drug consumption, and social behavior in comparison with patients presenting only DGR. The study included 560 patients with primary DGR on endoscopy divided into two groups, according to the presence/absence of H. pylori infection on biopsy (utilizing usual stainings and immunohistochemical methods). There was no significant difference in terms of age and sex, nor in the frequency of diabetes or esophagitis between the studied groups. Epigastric pain was associated with H. pylori-positive biopsies in multivariate logistic regression analysis (P=0.005). Although without statistical significance, severe endoscopic lesions and premalignant gastric lesions were more frequent in the H. pylori group (45.1 vs. 28.4% and 37.4 vs. 32.3%, respectively). In patients with DGR, the final multivariate model revealed a positive association between smoking and immunohistochemically confirmed H. pylori infection (P=0.02, OR=1.88, 95% confidence intervals (CI)=1.10 to 3.21), but a negative effect of proton pump inhibitor consumption (P<0.001, OR=0.50, 95% CI=0.35 to 0.73). In conclusion, in patients with H. pylori infection and DGR, epigastric pain was the main reason for the endoscopic investigation. H. pylori infection over DGR did not influence the severity of endoscopic or premalignant gastric lesion development. Furthermore, smoking is directly related to immunohistochemically assessed active H. pylor i infection in patients with bile reflux.

PMID:34055065 | PMC:PMC8145345 | DOI:10.3892/etm.2021.10198

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Risk factors for positive sentinel lymph node, lymphatic or hematogenous dissemination over time in patients with cutaneous melanoma

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Exp Ther Med. 2021 Jul;22(1):730. doi: 10.3892/etm.2021.10162. Epub 2021 May 5.

ABSTRACT

The aim of the present study was to assess the influence of localization, age or sex and histopathological characteristics upon the chance of developing lymphatic or hematogenous metastatic spread over time, or a positive sentinel lymph node in cutaneous melanoma patients. Patients from the Department of Dermatology, County Emergency Hospital Cluj-Napoca (Cluj-Napoca, Romania), presenting with cutaneous melanoma confirmed histopathologically and a SPECT/CT or lymphoscintigraphic examination to detect the sentinel lymph node, were included in the present study. Our results revealed that Breslow index >2 mm [odds ratio (OR)=4.22, 95% confidence interval (CI) (1.12; 15.93)], presence of ulceration [OR=6.01, 95% CI (1.87; 19.35)], and positive sentinel lymph node [for at least one sentinel lymph node OR=3.58, 95% CI (1.06; 12.04)] were risk factors for hematogenous metastases. All these, except for the Breslow index >2 mm, were demonstrated to be a risk factor for lymphatic spread metastases over time. Ulceration and male sex also represented risk factors for a positive sentinel lymph node, men having a higher risk of developing sentinel lymph nodes than women [adjusted OR=2.27, 95% CI (1.00; 5.13)]. In conclusion, the predictors that influence the occurrence of lymphatic or hematogenous metastases may differ, ulceration and positive sentinel lymph node being common for both types of metastatic spread, while Breslow index being a significant predictor only for hematogenous metastases. Male sex and the presence of ulceration were demonstrated to be significant risk factors for positive sentinel lymph nodes.

PMID:34055049 | PMC:PMC8145265 | DOI:10.3892/etm.2021.10162

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Silencing of kallikrein-related peptidase 6 attenuates the proliferation, migration, and invasion of gastric cancer cells through inhibition of epithelial-mesenchymal transition

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Exp Ther Med. 2021 Jul;22(1):770. doi: 10.3892/etm.2021.10202. Epub 2021 May 17.

ABSTRACT

Kallikrein-related peptidase 6 (KLK6), a member of the kallikrein-related peptidase family, is involved in the regulation of epithelial-mesenchymal transition (EMT) in cancer cells and is highly expressed in gastric cancer tissues. The aim of the present study was to investigate the effect of KLK6 on the proliferation, migration and invasion of gastric cancer cells and to determine the underlying mechanism of its actions. The expression of KLK6 was measured in metastatic gastric cancer cells using western blotting and reverse transcription-quantitative PCR, and KLK6 was overexpressed or inhibited in HGC-27 cells using plasmid transfection. Cell proliferation, migration, invasion and EMT were also evaluated using Cell Counting Kit 8, Transwell and western blot analysis, respectively. In addition, a mouse xenograft model was constructed by injection of HGC-27 cells. The xenograft was treated with KLK6 interference or overexpression plasmids to study the in vivo effects of KLK6 on tumor development. The results demonstrated that KLK6 was highly expressed in HGC-27 cells and that KLK6 inhibition attenuated cell proliferation, migration and invasion and prevented gastric cancer tumor development. In addition, KLK6 inhibition reduced the expression of epithelial cell adhesion molecule and vimentin, reduced the phosphorylation of SMAD2 and SMAD3 and upregulated epithelial-cadherin expression. In conclusion, KLK6 inhibition suppressed the proliferation, migration and invasion of gastric cancer cells both in vitro and in vivo through the inhibition of EMT. These findings indicate that KLK6 a potential therapeutic target for gastric cancer therapy.

PMID:34055069 | PMC:PMC8145264 | DOI:10.3892/etm.2021.10202

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lncRNA WT1-AS is upregulated in osteoporosis and regulates the apoptosis of osteoblasts by interacting with p53

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Exp Ther Med. 2021 Jul;22(1):734. doi: 10.3892/etm.2021.10166. Epub 2021 May 9.

ABSTRACT

In cervical cancer, cellular tumor antigen p53 (p53) interacts with long non-coding WT1 antisense RNA (WT1-AS) and this protein serves an important role in osteoporosis. The present study aimed to investigate the role of WT1-AS in osteoporosis. WT1-AS was upregulated in the plasma of patients with osteoporosis and was positively correlated with p53 expression. Altered expression of WT1-AS and p53 separated patients with osteoporosis from healthy controls. Expression levels of WT1-AS and p53 decreased with prolonged treatment. In osteoblasts, WT1-AS overexpression resulted in increased p53 expression, while WT1-AS small interfering RNA (siRNA) silencing resulted in decreased p53 expression. In addition, WT1-AS overexpression resulted in increased apoptosis rate, while WT1-AS siRNA silencing resulted in decreased apoptosis rate in osteoblasts. p53 ov erexpression attenuated the effects of WT1-AS siRNA silencing on cell apoptosis. Therefore, WT1-AS was upregulated during osteoporosis and regulated the apoptosis of osteoblasts by interacting with p53.

PMID:34055051 | PMC:PMC8138279 | DOI:10.3892/etm.2021.10166

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Oxidative stress and peripartum outcomes (Review)

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Exp Ther Med. 2021 Jul;22(1):771. doi: 10.3892/etm.2021.10203. Epub 2021 May 17.

ABSTRACT

Pregnancy, labor and childbirth are accompanied by excessive oxidative aggression. The excessive formation of free radicals [reactive oxygen species (ROS), reactive nitrogen species (RNS), chlorine reactive species (CRS)] causes cellular oxidative damage, which can be scavenged by enzymatic or non-enzymatic antioxidants in normal healthy pregnancy, physiological labor and delivery without any complications. An imbalance between the pro-oxidant and antioxidant factors may lead to oxidative stress, which contributes to the development of many diseases. This oxidative aggression can be a precursor for pathologies in the pregnant woman including eclampsia, miscarriage, preterm labor, and intrauterine growth retardation; in the offspring it may lead to bronchopulmonary dysplasia/chronic lung disease, necrotizing enterocolitis, retinopathy of prematurit y, and periventricular leukomalacia. This review summarizes the studies conducted to identify the mechanisms of oxidative stress and the effect of cell membrane oxidation, the mechanisms that are behind oxidative stress-related diseases, and also those studies which have demonstrated the effect of antioxidants in preventing diseases or diminishing the effects of oxidative stress in the body, in obstetrics and neonatology.

PMID:34055070 | PMC:PMC814 5513 | DOI:10.3892/etm.2021.10203

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Bcl-xL mutant promotes cartilage differentiation of BMSCs by upregulating TGF-β/BMP expression levels

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Exp Ther Med. 2021 Jul;22(1):736. doi: 10.3892/etm.2021.10168. Epub 2021 May 9.

ABSTRACT

Bcl-xL is a transmembrane molecule in the mitochondria, with apoptosis-related and pro-metabolic functions, that also plays a role in chondrogenesis and differentiation. A Bcl-xL mutant, in which the GRI sequence is replaced by ELN, has no anti-apoptotic effect, while other biological functions of this mutant remain unchanged. The present study investigated the impact of this Bcl-xL mutant on cartilage differentiation and the expression levels of TGF-β and bone morphogenetic protein (BMP). Human bone marrow mesenchymal stem cells (BMSCs) were transfected with Bcl-xL and Bcl-xL mutant (∆Bcl-xL) overexpression vectors. The cells were divided into four groups: Control (not subjected to any transfection), EV (empty pcDNA3.1-Bcl-xL vector), OV (Bcl-xL overexpression) and ∆OV (∆Bcl-xL overexpression). Saffron and toluidine blue staining was perfor med to observe cartilage tissue formation. Flow cytometry was conducted to measure BMSC apoptosis. The expression levels of TGF-β and BMP were evaluated using reverse transcription-quantitative PCR (RT-qPCR) and western blotting. Compared with that in the control group, the expression levels of Bcl-xL in the OV group increased significantly (P<0.05). Western blotting and RT-qPCR results revealed that OV and ∆OV treatment increased the expression levels of TGF-β and BMP in transfected cells, compared to their expression in the control and EV groups (P<0.05). Saffron and toluidine blue staining results showed that cartilage formation was increased in the ∆OV and ∆OV + Bax-/Bak-groups to similar degrees. Cell apoptosis in the ∆OV group did not change compared with that in the control group. The Bcl-xL mutant promoted cartilage differentiation of BMSCs and upregulated TGF-β/BMP expression. This enhancement of chondrogenic differentiation was not related to the expressio n of Bax and Bak. Taken together, these findings provided for improved application of bone tissue engineering technology in the treatment of articular cartilage defects.

PMID:34055053 | PMC:PMC8138271 | DOI:10.3892/etm.2021.10168

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