Two neonates, one 15 days old and another 20 days old, presented with redness, eye watering, periocular and lid
swelling, photophobia, and vesicular lesions over forehead on the right side of face. Ocular examination revealed
ciliary and conjunctival congestion, chemosis, and hazy cornea due to stromal edema. Although herpes zoster is
very rare in neonates, the diagnosis of herpes zoster ophthalmicus was made and treated with systemic and topical antiviral, topical antibiotic, and corticosteroid. Both neonates showed dramatic response in 7 days of treatment and fully cured within 4 weeks.
Contact Lens Peripheral Ulcer - Case Reportpaymaun19
Contact lens peripheral ulcer (CLPU) is a corneal ulcer that is stimulated from contact lens wear. Despite advancement in contact lens properties, patients are still at risk of developing contact lens-related complications. Even for the most hygienic and compliant contact lens patients, complications can still occur. Although the nature of CLPU is typically not sight-threatening, understanding the pathophysiology of CLPU is important and requires immediate management and monitoring. This case will outline a discussion involving the treatment and management for contact lens peripheral ulcer (CLPU).
ABSTRACT- A prospective case study of patients presenting with clinically suspected keratitis was conducted at Al-Rehma Hospital, Sirte, Libya between January 2008 and November 2010. A total of 32.9% patients were identified with fungal keratitis, Aspergillus and Fusarium together accounted for 89.28% of cases. Males had higher predisposition as compared with females. Trauma (78.5%) was the major cause, vegetative injury alone constituting 60.7% of cases. Other most common identifiable risk factors were history of diabetes mellitus (17.8%), contact lens (21.4%) and corticosteroids (3.57%). Fungal keratitis still possesses a significant threat for increased ocular morbidity. The overall knowledge of fungal keratitis with its clinical determinants and risk factors, would aid in general awareness and prevention of complications associated with it.
Key-words- Fungal keratitis, Cornea, Vegetative trauma, Contact lens, Diabetes mellitus, Corticosteroid
Sebaceous Carcinoma Masquerading As Chronic BlepharoconjunctivitisNot Relevant
Conjunctival intraepithelial neoplasia and sebaceous cell carcinoma have been reported to show intraepithelial
(pagetoid) spread to the conjunctiva mimicking chronic blepharoconjunctivitis, or cicatrizing conjunctivitis.
Esen Karamursel Akpek, MD
Contact Lens Peripheral Ulcer - Case Reportpaymaun19
Contact lens peripheral ulcer (CLPU) is a corneal ulcer that is stimulated from contact lens wear. Despite advancement in contact lens properties, patients are still at risk of developing contact lens-related complications. Even for the most hygienic and compliant contact lens patients, complications can still occur. Although the nature of CLPU is typically not sight-threatening, understanding the pathophysiology of CLPU is important and requires immediate management and monitoring. This case will outline a discussion involving the treatment and management for contact lens peripheral ulcer (CLPU).
ABSTRACT- A prospective case study of patients presenting with clinically suspected keratitis was conducted at Al-Rehma Hospital, Sirte, Libya between January 2008 and November 2010. A total of 32.9% patients were identified with fungal keratitis, Aspergillus and Fusarium together accounted for 89.28% of cases. Males had higher predisposition as compared with females. Trauma (78.5%) was the major cause, vegetative injury alone constituting 60.7% of cases. Other most common identifiable risk factors were history of diabetes mellitus (17.8%), contact lens (21.4%) and corticosteroids (3.57%). Fungal keratitis still possesses a significant threat for increased ocular morbidity. The overall knowledge of fungal keratitis with its clinical determinants and risk factors, would aid in general awareness and prevention of complications associated with it.
Key-words- Fungal keratitis, Cornea, Vegetative trauma, Contact lens, Diabetes mellitus, Corticosteroid
Sebaceous Carcinoma Masquerading As Chronic BlepharoconjunctivitisNot Relevant
Conjunctival intraepithelial neoplasia and sebaceous cell carcinoma have been reported to show intraepithelial
(pagetoid) spread to the conjunctiva mimicking chronic blepharoconjunctivitis, or cicatrizing conjunctivitis.
Esen Karamursel Akpek, MD
The important diseases recognized as responsible for visual impairment and blindness in India are cataract, refraction errors, glaucoma, conjunctivitis.
Mal nutrition and systemic disease are also important contributing factors.
Other causes include are eye injury, congenital disorders, retinal detachment, tumors, leprosy etc.
The visual disorder can be found as the following problems.
Amblyopia or subnormal vision in one or both eyes in spite of correction of significant refractive error.
Night blindness – it means inability to well at night or in faint light. It may occur in retinitis, choroidoretinistis, Vit A deficiency, retina toxic drugs.
Double Vision – It is found in squint, ptosis. It may be warning sign of increase IOP, brain tumor, orbital or myasthenia gravis.
Color blindness – It is a genetically determine condition in which color perception is defective or absent. Red and green color deficiency is the usual found. It can be detected at the age of 5 to 6 years’ age.
It is found in about 8% of the male population and is inherited as sex linked recessive trait. Color blindness may be total or partial there is no specific treatment.
Some main responsible disease for visual impairments in India :-
Conjunctivitis
Cataract
Refractory errors
Glaucoma
Retinopathy of Prematurity
OCULAR VIRAL ILLNESSES with different ocular manifestationsBARNABASMUGABI
it entails a description of the ocular manifestations of various viral infections and their management aswell as their complications and how to go about the complications
Purpose: We report a rare case of a 2 - year-old child with ectopia lentis and potential Marfan syndrome (MFS) and discuss her management.
Methods: A 2 - year - old female with no signifi cant past medical history was brought in by her mother after complaints that the child has recently been holding everything close to her eyes while simultaneously shifting her head down. Her mother reported no history of pain or trauma. The child’s family history was negative for ectopia lentis or MFS.
The corneal diseases are one of the leading causes of blindness in the world. in most cases, these infections are preventable or treatable.
This seminar provides an overview of the anatomy and physiology of the cornea, as well as an overview of common conditions.
Crouzon syndrome is the most common syndrome in the craniosynostosis group. Crouzon syndrome accounts for about 4.8 of all cases. It usually has autosomal dominant inheritance with full penetrance and variable expressiveness from subtle to severe forms and is caused by maxillary hypoplasia with craniosynostosis, proptosis, and relative mandibular protrusion. be characterized. Mutations in the fibroblast growth factor receptor 2 gene have been implicated in the development of this rare genetic disorder. Our work reports the diagnosis of this rare syndrome in young patients based on clinical and radiological features. Prompt and timely treatment of the syndrome has allowed this patient to lead a normal life despite the syndrome. Dr. Kala Barathi. S | Mr. Azrudheen. B "Crouzon Syndrome: A Case Report" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-7 | Issue-1 , February 2023, URL: https://www.ijtsrd.com/papers/ijtsrd53851.pdf Paper URL: https://www.ijtsrd.com/medicine/nursing/53851/crouzon-syndrome-a-case-report/dr-kala-barathi-s
a double-stranded DNA virus : human herpesvirus-3 subfamily Alphaherpersvirinae
only one serotype is known
humans are the only reservoir
VZV enters the host through the nasopharyngeal mucosa, and almost invariably produces clinical disease in susceptible individuals
Following varicella, the virus persists in sensory nerve ganglia, from where it may later be reactivated to cause herpes zoster (Shingles)
Types of viral keratitis, diagnosis of different types and management of each. Clinical evaluation with images described. Standard treatment protocols given.
A case of fusional vergence disorder associated with myopiaBIJCROO
Aim: This case study demonstrates the management options for fusional vergence dysfunction (FVD) and
uncorrected myopia.
Background: Binocular vision disorder with abnormalities in fusional vergence dynamics is referred to as “fusional
vergence dysfunction (FVD).” A patient with FVD has asthenopic symptoms, no refractive error, healthy eyes,
normal accommodative functions, a normal accommodative convergence/accommodation ratio, and normal
distant and near phoria status.
Case presentation: A 19-year-old female diagnosed to have FVD along with simple myopia presented to the
clinic with a complaint of asthenopic symptoms. Complete vergence-related and accommodation-related vision
therapies were advised and provided. After 2 months from the initial presentation, the patient successfully
recovered from the existing condition.
Conclusion: Uncorrected myopia with FVD was determined based on the patient’s complaint and the results of
the examination. The condition was treated with vision therapy and a distance optical correction. An office-based
and home-based program can successfully cure FVD
Smartphone – a third eye of people with blindnessBIJCROO
In the current plethora of the digital world, smartphones
have become an integral part of our lives and act as an
essential supportive device in executing daily living activities.
Until now, most of us believe that smartphones are devices
meant for people with a good sight and are not considered
assistive devices for visually impaired individuals. It may
not be an incorrect statement, particularly in lower-middleincome countries. It is a common presumption that the
use of smartphones would need a good vision function,
or how can they be used by people with vision loss?
However, in the recent past, technological advancement
has led to makeshift changes in the interfaces between
humans and smartphones in terms of interaction
More Related Content
Similar to Neonatal herpes zoster ophthalmicus: Two rare cases
The important diseases recognized as responsible for visual impairment and blindness in India are cataract, refraction errors, glaucoma, conjunctivitis.
Mal nutrition and systemic disease are also important contributing factors.
Other causes include are eye injury, congenital disorders, retinal detachment, tumors, leprosy etc.
The visual disorder can be found as the following problems.
Amblyopia or subnormal vision in one or both eyes in spite of correction of significant refractive error.
Night blindness – it means inability to well at night or in faint light. It may occur in retinitis, choroidoretinistis, Vit A deficiency, retina toxic drugs.
Double Vision – It is found in squint, ptosis. It may be warning sign of increase IOP, brain tumor, orbital or myasthenia gravis.
Color blindness – It is a genetically determine condition in which color perception is defective or absent. Red and green color deficiency is the usual found. It can be detected at the age of 5 to 6 years’ age.
It is found in about 8% of the male population and is inherited as sex linked recessive trait. Color blindness may be total or partial there is no specific treatment.
Some main responsible disease for visual impairments in India :-
Conjunctivitis
Cataract
Refractory errors
Glaucoma
Retinopathy of Prematurity
OCULAR VIRAL ILLNESSES with different ocular manifestationsBARNABASMUGABI
it entails a description of the ocular manifestations of various viral infections and their management aswell as their complications and how to go about the complications
Purpose: We report a rare case of a 2 - year-old child with ectopia lentis and potential Marfan syndrome (MFS) and discuss her management.
Methods: A 2 - year - old female with no signifi cant past medical history was brought in by her mother after complaints that the child has recently been holding everything close to her eyes while simultaneously shifting her head down. Her mother reported no history of pain or trauma. The child’s family history was negative for ectopia lentis or MFS.
The corneal diseases are one of the leading causes of blindness in the world. in most cases, these infections are preventable or treatable.
This seminar provides an overview of the anatomy and physiology of the cornea, as well as an overview of common conditions.
Crouzon syndrome is the most common syndrome in the craniosynostosis group. Crouzon syndrome accounts for about 4.8 of all cases. It usually has autosomal dominant inheritance with full penetrance and variable expressiveness from subtle to severe forms and is caused by maxillary hypoplasia with craniosynostosis, proptosis, and relative mandibular protrusion. be characterized. Mutations in the fibroblast growth factor receptor 2 gene have been implicated in the development of this rare genetic disorder. Our work reports the diagnosis of this rare syndrome in young patients based on clinical and radiological features. Prompt and timely treatment of the syndrome has allowed this patient to lead a normal life despite the syndrome. Dr. Kala Barathi. S | Mr. Azrudheen. B "Crouzon Syndrome: A Case Report" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-7 | Issue-1 , February 2023, URL: https://www.ijtsrd.com/papers/ijtsrd53851.pdf Paper URL: https://www.ijtsrd.com/medicine/nursing/53851/crouzon-syndrome-a-case-report/dr-kala-barathi-s
a double-stranded DNA virus : human herpesvirus-3 subfamily Alphaherpersvirinae
only one serotype is known
humans are the only reservoir
VZV enters the host through the nasopharyngeal mucosa, and almost invariably produces clinical disease in susceptible individuals
Following varicella, the virus persists in sensory nerve ganglia, from where it may later be reactivated to cause herpes zoster (Shingles)
Types of viral keratitis, diagnosis of different types and management of each. Clinical evaluation with images described. Standard treatment protocols given.
A case of fusional vergence disorder associated with myopiaBIJCROO
Aim: This case study demonstrates the management options for fusional vergence dysfunction (FVD) and
uncorrected myopia.
Background: Binocular vision disorder with abnormalities in fusional vergence dynamics is referred to as “fusional
vergence dysfunction (FVD).” A patient with FVD has asthenopic symptoms, no refractive error, healthy eyes,
normal accommodative functions, a normal accommodative convergence/accommodation ratio, and normal
distant and near phoria status.
Case presentation: A 19-year-old female diagnosed to have FVD along with simple myopia presented to the
clinic with a complaint of asthenopic symptoms. Complete vergence-related and accommodation-related vision
therapies were advised and provided. After 2 months from the initial presentation, the patient successfully
recovered from the existing condition.
Conclusion: Uncorrected myopia with FVD was determined based on the patient’s complaint and the results of
the examination. The condition was treated with vision therapy and a distance optical correction. An office-based
and home-based program can successfully cure FVD
Smartphone – a third eye of people with blindnessBIJCROO
In the current plethora of the digital world, smartphones
have become an integral part of our lives and act as an
essential supportive device in executing daily living activities.
Until now, most of us believe that smartphones are devices
meant for people with a good sight and are not considered
assistive devices for visually impaired individuals. It may
not be an incorrect statement, particularly in lower-middleincome countries. It is a common presumption that the
use of smartphones would need a good vision function,
or how can they be used by people with vision loss?
However, in the recent past, technological advancement
has led to makeshift changes in the interfaces between
humans and smartphones in terms of interaction
Accommodative facility and vergence facility after mobile gamingBIJCROO
Aim: This study aimed to access the changes of accommodation and vergence before and after mobile gaming.
Settings and Design: This was a comparative study conducted in the outpatient department of ophthalmology.
Accommodative facility and vergence facility were measured using flippers.
Materials and methods: A comparative study was conducted on 50 healthy subjects, in both males and females,
with age groups ranging between 18 and 30 years. This study has been approved by the IRB Committee; 25 young
emmetropic patients and 25 young myopic patients were included. The comparison of accommodative facility
and vergence facility before and after mobile gaming for 1 h was measured to determine the level of changes
in accommodation and vergence. All patients were undergone comprehensive ophthalmic examination including
vision, subjective/objective refraction, anterior segment examination, and accommodative and vergence facilities
measured using accommodative and vergence flippers.
Results: The mean and standard deviation value significantly increase before and after mobile gaming in the right
eye, left eye, and both eyes in case of accommodation facility, and there is a decrease in the mean and standard
deviation value in case of vergence facility in both eyes before and after mobile gaming.
Conclusion: The mean and standard deviation value significantly increase before and after mobile gaming in the
right eye, left eye, and both eyes in case of accommodative facility, and there is a decrease in the mean and standard deviation value in case of vergence facility in both eyes before and after mobile gaming.
Phenotypic analysis of a case of “3MC syndrome” with review of literatureBIJCROO
3MC syndrome is a very rare entity. Its prevalence is unknown, but most cases are reported from the Middle East.
The first case was reported in 1978 and named as Michels syndrome, and recently, with other three syndromes
together, these syndromes are named as 3MC syndrome. All are autosomal recessive disorders and have been
reported by both consanguineous and non-consanguineous parents. Here, we phenotypically analyzed a case presented with the features of blepharophimosis syndrome associated with craniosynostosis suggestive of Michel syndrome, which is a part of the “3MC syndrome.”
A case of Alport syndrome presented with bilateral anterior lenticonusBIJCROO
Purpose: The aim of this study was to report a rare case of Alport syndrome presented with bilateral anterior
lenticonus in a 16-year-old boy.
Case report: A 16-year-old boy presented with decreased vision, a hearing defect, anemia, and proteinuria. His
best corrected visual acuity was 6/18 in both eyes. Slit lamp biomicroscope showed anterior lenticonus in both
eyes. He was managed by correction of refractive error and urgent referral to a nephrologist.
Conclusion: It is easy to diagnose Alport syndrome clinically, and close communication among ophthalmologists,
otorhinolaryngologists, and nephrologists is crucial for effective management of this syndrome.
Smoking and alcoholism: Risk factors for papillitis?BIJCROO
Introduction: Papillitis is the inflammation of the optic nerve at the level of the optic papilla or optic disc. We did
not find enough published studies that corroborate smoking and alcoholism as absolute risk factors for papillitis;
however, it has been raised, so we were motivated to conduct this research, with the aim of identifying a statistically
significant causal association between these factors and papillitis in our hospital.
Methodology: An analytical study of cases and controls was carried out in patients with papillitis treated at the
Ophthalmology Centre of Santiago de Cuba (2017–2019). Group 1 (cases): 42 patients; group 2 (controls): 84
patients’ companions who attended in the same period and did not present ophthalmological entities.
Results: In the association of smoking with papillitis, we obtained an odds ratio (OR) = 1.60, with confidence
interval (CI): [0.74; 3.48], but p > 0.05. Alcoholism with papillitis resulted in an association with OR = 1.19, with CI:
[0.53; 2.68] and p > 0.05.
Conclusion: In this study, smoking and alcoholism had no statistically significant causal association with papillitis.
Megalocornea-mental retardation syndrome: Rare but can be thereBIJCROO
We report a case study of a 10-year-old male who had megalocornea with mental retardation (Neuhäuser
syndrome). Megalocornea-mental retardation is a rare syndrome with a few cases reported in literature. The patientwith megalocornea-mental retardation requires a thorough systemic examination.
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Neonatal herpes zoster ophthalmicus: Two rare cases
1. BOHR International Journal of Current Research
in Optometry and Ophthalmology
2022, Vol. 1, No. 1, pp. 11–13
DOI: 10.54646/bijcroo.2022.04
www.bohrpub.com
CASE STUDY
Neonatal herpes zoster ophthalmicus: Two rare cases
Sujit Kumar Biswas*, Soma Rani Roy and ASM Mahbubul Alam
Department of Cornea, Chittagong Eye Infirmary and Training Complex, Chattogram, Bangladesh
*Correspondence:
Sujit Kumar Biswas,
dr.sujitkumar2020@gmail.com
Received: 24 February 2022; Accepted: 04 March 2022; Published: 15 March 2022
Two neonates, one 15 days old and another 20 days old, presented with redness, eye watering, periocular and lid
swelling, photophobia, and vesicular lesions over forehead on the right side of face. Ocular examination revealed
ciliary and conjunctival congestion, chemosis, and hazy cornea due to stromal edema. Although herpes zoster is
very rare in neonates, the diagnosis of herpes zoster ophthalmicus was made and treated with systemic and topical
antiviral, topical antibiotic, and corticosteroid. Both neonates showed dramatic response in 7 days of treatment
and fully cured within 4 weeks.
Keywords: herpes zoster, child hood zoster, varicella zoster, post herpetic neuralgia
Introduction
Herpes ophthalmicus (HZO) is a result of reactivated
varicella-zoster virus (VZV) (1). HZO is rare in neonates.
Usually, neonatal HZO is associated with history of maternal
infection of varicella-zoster infection (chickenpox) during
pregnancy. Early neonatal varicella (chickenpox) due to
weak immune system is more likely to result in childhood
zoster (2). Neonatal HZO is frequently misdiagnosed as
impetigo or other cutaneous disorders as it presents with
mild clinical manifestations.
Case 1
A 15-day-old baby girl from a low socioeconomic society
presented at Cornea Clinic with the complaints of redness,
eye watering, eyelids and periocular swelling, intolerance
to light, and elevated spots in the forehead, scalp, and
tip of the nose on the right side of face for 5 days.
There was no history of maternal chickenpox and no
history of varicella vaccination of mother during pregnancy.
Examination revealed vesiculopapular rashes and pastules
over the right side of forehead, scalp, and tip of the
nose (Hutchinson’s sign) along with the right cranial
nerve V-1 dermatome, mild edema of lids with matted
eyelashes, ciliary and conjunctival congestion, conjunctival
chemosis, hazy cornea due to stromal edema, round,
regular and reacting pupil, and deep anterior chamber
with clear lens. Her left eye was normal and she was
afebrile. Tzanck smear, serology, and viral culture were
not performed. She was diagnosed clinically as HZO and
treated with homatropine eye drops 2%, 3 times daily;
moxifloxacin eye drops 0.3%, 4 times daily; acyclovir
eye ointment 3%, 5 times daily; dexamethasone eye
drops 0.1%, 4 times daily in her right eye; mupirocin
skin ointment 2 times daily over vesiculopastular lesions;
and oral acyclovir (syrup) 30 mg/kg body weight in 3
divided doses for 7 days. Dramatic response resulted
after 7 days. Vesiculopapular rashes and pastules nearly
resolved, ciliary and conjunctival congestion was diminished,
cornea became clear. Acyclovir eye ointment 3% and
dexamethasone eye drops 0.1% were tapered over a month.
The baby was good and no recurrence in 5 years follow-
up (Figure 1).
Case 2
A 20-day-old baby boy presented to cornea department
with vesicular lesion over the right side of forehead and
eye watering, lid swelling, and photophobia of the right
eye for 3–4 days. History of maternal chickenpox during
11
2. 12 Biswas et al.
FIGURE 1 | (A) Papulovesicular rashes over forehead and positive Hutchinson’s sign. (B) Stromal keratitis. (C) Resolved rashes after 4 weeks.
(D) Resolved stromal keratitis with clear cornea.
pregnancy and varicella vaccination of mother in pregnancy
were absent. Examination revealed vesiculopustular lesion
over the right forhead not crossing the midline, swelling of
lid with discharge and excoriation of margin, conjunctival
and ciliary congestion, and stromal keratitis without irs
detail. His other eye was normal, patient was afebrile,
and there was no other systemic abnormality. The baby
was diagnosed as HZO of the right eye based on clinical
features and treated with topical homatropine eye drops
2%, three times daily; moxifloxacin eye drops 0.3%, 4
times daily; ganciclovir eye ointment 0.15%, 5 times
daily; dexamethasone eye drops 0.1%, 4 times daily
in her right eye; mupirocin skin ointment two times
daily over vesiculopastular lesions; and oral acyclovir
(syrup) 30 mg/kg body weight in 3 divided doses for
7 days. Parent was asked for follow-up after 7 days but
presented after 14 days. Vesiculopapular rashes and
pastules were resolved, and only scar was over forehead,
ciliary and conjunctival congestion reduced, and cornea
became clear. Ganciclovir eye ointment 0.15% and
dexamethasone eye drops 0.1%, were tapered over a
month. The patient was in good health up to 2 years
follow-up (Figure 2).
Discussion
Herpes zoster ophthalmicus is more common in adults than
children, but it may occur as early as the first year of life.
Globally, the age-adjusted incidence rate of herpes zoster
is the lowest (0.45 per 1000 person-years) in 0–14 years
age group and highest (4.2–4.5 per 1000 person-years)
among people aged 75 years and older (3). In the pediatric
population, the incidence is the lowest in 0–5 years age group
(20 per 100 000 person-years) compared with adolescents
(63 per 100 000 person-years) (4). In children who develop
zoster in the first 2 years of life, there is rarely a history
of chickenpox but a history of maternal chickenpox during
pregnancy is found. Early neonatal varicella (chickenpox)
due to weak immune system is more likely to result in
childhood zoster. In a few instances, primary infections
by VZV appear to provoke zoster rather than chickenpox,
3. 10.54646/bijcroo.2022.04 13
FIGURE 2 | (A) Vesiculopastular rashes over forehead and periocular area. (B) Stromal keratitis associated with lid margin excoriation.
(C) Resolved rashes with scar after 4 weeks. (D) Resolved stromal keratitis with clear cornea.
but the explanation is not known. On occasion, zoster
may also occur simultaneously with a primary attack
of chickenpox. Postherpetic neuralgia, which is common
in affected adults, rarely occur in childhood (2). Herpes
zoster in children represents an uncommon finding with
potentially devastating sequelae. The incidence of childhood
zoster is 122 times higher in children with a childhood
malignancy. Varicella vaccination can also be a risk factor
for development of infection because current vaccines are
made from live-attenuated viruses (5). The most frequent
cause in immunocompetent patients is intrauterine exposure
to VZV. It has been hypothesized that this condition is rarely
recognized because of the mild clinical manifestations in
this age group and the expectation that maternal antibodies
will be protective (6). It is likely that the vesicular lesions
of herpes zoster in this age group are misdiagnosed as
impetigo or other cutaneous disorders. With a high degree
of suspicion, the dermatomal distribution of a vesicular
eruption in infancy should point the clinician toward a
correct diagnosis of herpes zoster (7).
We believe that in our country HZO in neonates, although
not commonly reported, occurs more commonly than
expected due to poor immunity, mild clinical manifestation,
misdiagnosed as impetigo, and lack of investigations for
virus detection.
Conclusion
Herpes zoster ophthalmicus is very uncommon in neonate.
Dermatomal distribution of a vesicular eruption in infancy
strongly suggests the diagnosis of HZO and treatment with
systemic antiviral medication is generally satisfactory.
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