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The 2 closely related herpes simplex viruses (HSVs),
HSV type 1 (HSV-1) and HSV type 2 (HSV-2), cause a
variety of illnesses, depending on
the anatomic site where the infection is initiated,
the immune state of the host, and
whether the symptoms reflect primary or recurrent
infection.
Infections tend to be mild and self-limiting, except in
the immunocompromised patient and newborn infant,
in whom they may be severe and life-threatening.
Primary infection occurs in individuals who have not been
infected previously with either HSV-1 or HSV-2. Because these
individuals are HSV seronegative and have no preexisting
immunity to HSV, primary infections can be severe.
Nonprimary 1st infection occurs in individuals previously
infected with 1 type of HSV (e.g., HSV-1) who have become
infected for the 1st time with the other type of HSV (in this case,
HSV-2). Because immunity to 1 HSV type provides some cross
protection against disease caused by the other HSV type,
nonprimary 1st infections tend to be less severe than true
primary infections.
During primary and nonprimary initial infections, HSV
establishes latent infection in regional sensory ganglion
neurons. Virus is maintained in this latent state for the life
of the host but periodically can reactivate and cause
recurrent infection. Symptomatic recurrent infections
tend to be less severe and of shorter duration than 1st
infections.
Acute Oropharyngeal Infections
Herpes gingivostomatitis most often affects children
6 mo to 5 yr of age but is seen across the age spectrum.
It is an extremely painful condition with sudden onset,
 pain in the mouth
drooling
refusal to eat or drink
fever of up to 40.0-40.6°C (104-105.1°F)
markedly swollen gums
vesicles ((throughout the oral cavity, including the gums,lips,
tongue, palate, tonsils, pharynx, and perioral skin)) The vesicles are
generally present only a few days before progressing to form
shallow indurated ulcers that may be covered with a yellow-gray
membrane.
tonsillar exudates suggestive of bacterial pharyngitis.
Tender submandibular, submaxillary, and cervical
lymphadenopathy
foul smelling breath ((overgrowth of anaerobic oral bacteria))
the illness resolves in 7-14 days, although the
lymphadenopathy may persist for several weeks.
Herpes Labialis
Fever blisters (cold sores) are the most common
manifestation of recurrent HSV-1 infections. The most
common site of herpes labialis is the vermilion border of
the lip, although lesions sometimes occur on the nose,
chin, cheek, or oral mucosa.
Older patients report experiencing burning, tingling,
itching, or pain 3-6 hr (rarely as long as 24-48 hr) before
the development of the herpes lesion.
The lesion generally begins as a small grouping of
erythematous papules that over a few hours progress to
create a small, thin-walled vesicle. The vesicles may form
shallow ulcers or become pustular. The short-lived ulcer
dries and develops a crusted scab. Complete healing
without scarring occurs with reepithelialization of the
ulcerated skin, usually within 6-10 days. Some patients
experience local lymphadenopathy but no constitutional
symptoms.
Central Nervous System Infections
HSV encephalitis is the leading cause of sporadic, nonepidemic
encephalitis in children .It is an acute necrotizing infection involving the
frontal and/or temporal cortex and the limbic system The infection may
manifest as nonspecific findings
fever
headache
nuchal rigidity
Nausea & vomiting,
generalized or focal seizures
Altered consciousness
expressive aphasia
peculiar behavior
hallucinations
memory loss
anosmia
Beyond the neonatal period, is almost always caused by HSV-
1.
The untreated infection progresses to coma and death in 75%
of cases.
Examination of the cerebrospinal fluid (CSF) typically shows a
 moderate number of mononuclear cells and
polymorphonuclear leukocytes
mildly elevated protein concentration
normal or slightly decreased glucose concentration
moderate number of erythrocytes.
HSV is also a cause of aseptic meningitis and is the most
common cause of recurrent aseptic meningitis (Mollaret
meningitis).
Cutaneous Infections
In the healthy child or adolescent, cutaneous HSV
infections are generally the result of skin trauma with
macro or micro abrasions and exposure to infectious
secretions.
This situation most often occurs in play or contact
sports such as wrestling (herpes gladiatorum) and rugby
(scrum pox).
cutaneous HSV infection results in multiple discrete lesions
and involves a larger surface area.
Regional lymphadenopathy may occur but systemic
symptoms are uncommon.
Recurrences are sometimes associated with local edema and
lymphangitis or local neuralgia
Herpes whitlow is a term generally applied to HSV infection
of fingers or toes, it is most commonly seen in infants and
toddlers who suck the thumb or fingers and who are
experiencing either a symptomatic or a subclinical oral HSV-1
infection.
 An HSV-2 herpes whitlow occasionally develops in an
adolescent as a result of exposure to infectious genital
secretions.
 The onset of the infection is heralded by itching, pain, and
erythema 2-7 days after exposure. The cuticle becomes
erythematous and tender and may appear to contain pus,
although if it is incised, little fluid is present.
 Incising the lesion is discouraged, as this maneuver
typically prolongs recovery and increases the risk for secondary
bacterial infection.
 Lesions and associated pain typically persist for about 10
days, followed by rapid improvement and complete recovery in
18-20 days.
 Regional lymphadenopathy is common, and lymphangitis
and neuralgia may occur.
 Unlike other recurrent herpes infections, recurrent herpetic
whitlows are often as painful as the primary infection but are
generally shorter in duration.
 Cutaneous HSV infections can be severe or life-threatening
in patients with disorders of the skin such as
eczema (eczema herpeticum),
pemphigus
burns
Darier disease
following laser skin resurfacing.
 The lesions are frequently ulcerative and nonspecific in
appearance, although typical vesicles may be seen in adjacent
normal skin.
 If untreated, these lesions can progress to disseminated
infection and death. Recurrent infections are common but
generally less severe than the initial infection.
Infections in Immunocompromised Persons
 Severe, life-threatening HSV infections can occur in patients with
compromised immune functions, including
neonates
severely malnourished
primary or secondary immunodeficiency diseases, including AIDS
immunosuppressive regimens, particularly for cancer and organ
transplantation.
 Mucocutaneous infections, including mucositis and esophagitis, are
most common, although their presentations may be atypical. Other
HSV infections include tracheobronchitis, pneumonitis, and anogenital
infections.
 Disseminated infection can result in a sepsis-like presentation, with
liver and adrenal involvement, disseminated intravascular
coagulopathy, and shock.
DIAGNOSIS
The clinical diagnosis of HSV infections, particularly life-
threatening infections and genital herpes, should be confirmed
by laboratory test, preferably isolation of virus or viral DNA
detection by polymerase chain reaction (PCR).
 Virus culture remains the gold standard for diagnosing HSV
infections.
direct detection of HSV antigens in clinical specimens can be
done rapidly and has very good specificity.
PCR for detection of HSV DNA is highly sensitive and specific
and in some instances can be performed rapidly. It is the test of
choice in examining CSF in cases of suspected HSV encephalitis.
Because most HSV diagnostic tests take at least a few days
to complete, treatment should not be withheld but rather
initiated promptly so as to ensure the maximum
therapeutic benefit.
LABORATORY FINDINGS
Mucocutaneous infections may cause a moderate polymorphonuclear
Leukocytosis
meningoencephalitis CSF FINDINGS
1. moderate number of mononuclear cells and polymorphonuclear leukocytes
2. mildly elevated protein concentration
3. normal or slightly decreased glucose concentration
4. moderate number of erythrocytes.
EEG & MRI FINDINGS
Show temporal lobe abnormalities in HSV encephalitis beyond the neonatal period. in
the neonatal period tends to be more global and not limited to the temporal lobe
Disseminated infection
1. elevated liver enzymes
2. Thrombocytopenia
3. abnormal coagulation.
MANAGEMENT
gingivostomatitis
• oral acyclovir (15 mg/kg/dose 5 times a day PO for 7
days; maximum: 1 g/day) started within 72 hr of onset
reduces the severity and duration of the illness.
• Pain associated with swallowing may limit oral intake of
infants and children, putting them at risk for
dehydration.
•Intake should be encouraged through the use of cold
beverages, ice cream, and yogurt.
herpes labialis
Oral treatment is superior to topical antiviral therapy.
For treatment of a recurrence in adolescents,
•oral valacyclovir (2,000 mg bid PO for 1 day),
•acyclovir (200-400 mg 5 times daily PO for 5 days), or
•famciclovir (1,500 mg once daily PO for 1 day)
shortens the duration of the episode.
Long-term daily use of oral
• acyclovir (400 mg bid PO)
• valacyclovir (500 mg once daily PO)
has been used to prevent recurrences in individuals with
frequent or severe recurrences.
herpes gladiatorum
• oral acyclovir (200 mg 5 times daily PO for 7-10 days)
• valacyclovir (500 mg bid PO for 7-10 days)
with the first signs of the outbreak can shorten the course.
For recurrent herpes gladiatorum, chronic daily prophylaxis
with valacyclovir (500-1,000 mg daily) has been reported to
prevent recurrences.
herpetic whitlow
There are no clinical trials assessing the benefit of antiviral
treatment. High-dose oral acyclovir (1,600-2,000 mg/day divided
in 2-3 doses PO for 10 days) started at the first signs of illness
has been reported to abort some reoccurrences and reduce the
Central Nervous System Infections
Patients older than neonates who have herpes encephalitis
should be promptly treated with intravenous acyclovir (10
mg/kg every 8 hr given as a 1 hr infusion for 14-21 days).
Treatment for
•increased intracranial pressure,
•management of seizures, and
•respiratory compromise
may be required.
Infections in Immunocompromised Persons
•Severe mucocutaneous and disseminated HSV infections in
immunocompromised patients should be treated with
intravenous acyclovir (5-10 mg/kg or 250 mg/m2 every 8 hr)
until there is evidence of resolution of the infection.
•Oral antiviral therapy with acyclovir, famciclovir, or valacyclovir
has been used for treatment of less-severe HSV infections and
for suppression of recurrences during periods of significant
immunosuppression.
•Acyclovir-resistant viruses are often also resistant to famciclovir
but may be sensitive to foscarnet or cidofovir.
PROGNOSIS
Most HSV infections are self-limiting, last from a few days (for
recurrent infections) to 2-3 wk (for primary infections), and heal
without scarring.
Recurrent oral-facial herpes in a patient who has undergone
dermabrasion or laser resurfacing can be severe and lead to scarring.
Lifethreatening conditions include
•neonatal herpes
•herpes encephalitis
•HSV infections in immunocompromised patients
•burn patients
•severely malnourished infants and children.
Recurrent ocular herpes can lead to corneal scarring and blindness.
PREVENTION
oTransmission of infection occurs through exposure to virus either as
the result of skin-to-skin contact or from contact with contaminated
secretions.
oGood handwashing
ouse of gloves
oClean shared toys and athletic equipment such as wrestling mats at
least daily
after use
oUse of sun blockers is reported to be effective in preventing
orecurrent oral-facial herpes in patients with a history of sun-induced
recurrent disease.
Hsv , mazin malik

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Hsv , mazin malik

  • 1.
  • 2. The 2 closely related herpes simplex viruses (HSVs), HSV type 1 (HSV-1) and HSV type 2 (HSV-2), cause a variety of illnesses, depending on the anatomic site where the infection is initiated, the immune state of the host, and whether the symptoms reflect primary or recurrent infection. Infections tend to be mild and self-limiting, except in the immunocompromised patient and newborn infant, in whom they may be severe and life-threatening.
  • 3. Primary infection occurs in individuals who have not been infected previously with either HSV-1 or HSV-2. Because these individuals are HSV seronegative and have no preexisting immunity to HSV, primary infections can be severe. Nonprimary 1st infection occurs in individuals previously infected with 1 type of HSV (e.g., HSV-1) who have become infected for the 1st time with the other type of HSV (in this case, HSV-2). Because immunity to 1 HSV type provides some cross protection against disease caused by the other HSV type, nonprimary 1st infections tend to be less severe than true primary infections.
  • 4. During primary and nonprimary initial infections, HSV establishes latent infection in regional sensory ganglion neurons. Virus is maintained in this latent state for the life of the host but periodically can reactivate and cause recurrent infection. Symptomatic recurrent infections tend to be less severe and of shorter duration than 1st infections.
  • 5. Acute Oropharyngeal Infections Herpes gingivostomatitis most often affects children 6 mo to 5 yr of age but is seen across the age spectrum. It is an extremely painful condition with sudden onset,  pain in the mouth drooling refusal to eat or drink fever of up to 40.0-40.6°C (104-105.1°F) markedly swollen gums
  • 6. vesicles ((throughout the oral cavity, including the gums,lips, tongue, palate, tonsils, pharynx, and perioral skin)) The vesicles are generally present only a few days before progressing to form shallow indurated ulcers that may be covered with a yellow-gray membrane. tonsillar exudates suggestive of bacterial pharyngitis. Tender submandibular, submaxillary, and cervical lymphadenopathy foul smelling breath ((overgrowth of anaerobic oral bacteria)) the illness resolves in 7-14 days, although the lymphadenopathy may persist for several weeks.
  • 7.
  • 8. Herpes Labialis Fever blisters (cold sores) are the most common manifestation of recurrent HSV-1 infections. The most common site of herpes labialis is the vermilion border of the lip, although lesions sometimes occur on the nose, chin, cheek, or oral mucosa. Older patients report experiencing burning, tingling, itching, or pain 3-6 hr (rarely as long as 24-48 hr) before the development of the herpes lesion.
  • 9.
  • 10. The lesion generally begins as a small grouping of erythematous papules that over a few hours progress to create a small, thin-walled vesicle. The vesicles may form shallow ulcers or become pustular. The short-lived ulcer dries and develops a crusted scab. Complete healing without scarring occurs with reepithelialization of the ulcerated skin, usually within 6-10 days. Some patients experience local lymphadenopathy but no constitutional symptoms.
  • 11. Central Nervous System Infections HSV encephalitis is the leading cause of sporadic, nonepidemic encephalitis in children .It is an acute necrotizing infection involving the frontal and/or temporal cortex and the limbic system The infection may manifest as nonspecific findings fever headache nuchal rigidity Nausea & vomiting, generalized or focal seizures Altered consciousness expressive aphasia peculiar behavior hallucinations memory loss anosmia
  • 12. Beyond the neonatal period, is almost always caused by HSV- 1. The untreated infection progresses to coma and death in 75% of cases. Examination of the cerebrospinal fluid (CSF) typically shows a  moderate number of mononuclear cells and polymorphonuclear leukocytes mildly elevated protein concentration normal or slightly decreased glucose concentration moderate number of erythrocytes. HSV is also a cause of aseptic meningitis and is the most common cause of recurrent aseptic meningitis (Mollaret meningitis).
  • 13. Cutaneous Infections In the healthy child or adolescent, cutaneous HSV infections are generally the result of skin trauma with macro or micro abrasions and exposure to infectious secretions. This situation most often occurs in play or contact sports such as wrestling (herpes gladiatorum) and rugby (scrum pox).
  • 14.
  • 15. cutaneous HSV infection results in multiple discrete lesions and involves a larger surface area. Regional lymphadenopathy may occur but systemic symptoms are uncommon. Recurrences are sometimes associated with local edema and lymphangitis or local neuralgia
  • 16. Herpes whitlow is a term generally applied to HSV infection of fingers or toes, it is most commonly seen in infants and toddlers who suck the thumb or fingers and who are experiencing either a symptomatic or a subclinical oral HSV-1 infection.  An HSV-2 herpes whitlow occasionally develops in an adolescent as a result of exposure to infectious genital secretions.  The onset of the infection is heralded by itching, pain, and erythema 2-7 days after exposure. The cuticle becomes erythematous and tender and may appear to contain pus, although if it is incised, little fluid is present.
  • 17.
  • 18.  Incising the lesion is discouraged, as this maneuver typically prolongs recovery and increases the risk for secondary bacterial infection.  Lesions and associated pain typically persist for about 10 days, followed by rapid improvement and complete recovery in 18-20 days.  Regional lymphadenopathy is common, and lymphangitis and neuralgia may occur.  Unlike other recurrent herpes infections, recurrent herpetic whitlows are often as painful as the primary infection but are generally shorter in duration.
  • 19.  Cutaneous HSV infections can be severe or life-threatening in patients with disorders of the skin such as eczema (eczema herpeticum), pemphigus burns Darier disease following laser skin resurfacing.  The lesions are frequently ulcerative and nonspecific in appearance, although typical vesicles may be seen in adjacent normal skin.  If untreated, these lesions can progress to disseminated infection and death. Recurrent infections are common but generally less severe than the initial infection.
  • 20.
  • 21. Infections in Immunocompromised Persons  Severe, life-threatening HSV infections can occur in patients with compromised immune functions, including neonates severely malnourished primary or secondary immunodeficiency diseases, including AIDS immunosuppressive regimens, particularly for cancer and organ transplantation.  Mucocutaneous infections, including mucositis and esophagitis, are most common, although their presentations may be atypical. Other HSV infections include tracheobronchitis, pneumonitis, and anogenital infections.  Disseminated infection can result in a sepsis-like presentation, with liver and adrenal involvement, disseminated intravascular coagulopathy, and shock.
  • 22. DIAGNOSIS The clinical diagnosis of HSV infections, particularly life- threatening infections and genital herpes, should be confirmed by laboratory test, preferably isolation of virus or viral DNA detection by polymerase chain reaction (PCR).  Virus culture remains the gold standard for diagnosing HSV infections. direct detection of HSV antigens in clinical specimens can be done rapidly and has very good specificity. PCR for detection of HSV DNA is highly sensitive and specific and in some instances can be performed rapidly. It is the test of choice in examining CSF in cases of suspected HSV encephalitis.
  • 23. Because most HSV diagnostic tests take at least a few days to complete, treatment should not be withheld but rather initiated promptly so as to ensure the maximum therapeutic benefit.
  • 24. LABORATORY FINDINGS Mucocutaneous infections may cause a moderate polymorphonuclear Leukocytosis meningoencephalitis CSF FINDINGS 1. moderate number of mononuclear cells and polymorphonuclear leukocytes 2. mildly elevated protein concentration 3. normal or slightly decreased glucose concentration 4. moderate number of erythrocytes. EEG & MRI FINDINGS Show temporal lobe abnormalities in HSV encephalitis beyond the neonatal period. in the neonatal period tends to be more global and not limited to the temporal lobe Disseminated infection 1. elevated liver enzymes 2. Thrombocytopenia 3. abnormal coagulation.
  • 25. MANAGEMENT gingivostomatitis • oral acyclovir (15 mg/kg/dose 5 times a day PO for 7 days; maximum: 1 g/day) started within 72 hr of onset reduces the severity and duration of the illness. • Pain associated with swallowing may limit oral intake of infants and children, putting them at risk for dehydration. •Intake should be encouraged through the use of cold beverages, ice cream, and yogurt.
  • 26. herpes labialis Oral treatment is superior to topical antiviral therapy. For treatment of a recurrence in adolescents, •oral valacyclovir (2,000 mg bid PO for 1 day), •acyclovir (200-400 mg 5 times daily PO for 5 days), or •famciclovir (1,500 mg once daily PO for 1 day) shortens the duration of the episode. Long-term daily use of oral • acyclovir (400 mg bid PO) • valacyclovir (500 mg once daily PO) has been used to prevent recurrences in individuals with frequent or severe recurrences.
  • 27. herpes gladiatorum • oral acyclovir (200 mg 5 times daily PO for 7-10 days) • valacyclovir (500 mg bid PO for 7-10 days) with the first signs of the outbreak can shorten the course. For recurrent herpes gladiatorum, chronic daily prophylaxis with valacyclovir (500-1,000 mg daily) has been reported to prevent recurrences. herpetic whitlow There are no clinical trials assessing the benefit of antiviral treatment. High-dose oral acyclovir (1,600-2,000 mg/day divided in 2-3 doses PO for 10 days) started at the first signs of illness has been reported to abort some reoccurrences and reduce the
  • 28. Central Nervous System Infections Patients older than neonates who have herpes encephalitis should be promptly treated with intravenous acyclovir (10 mg/kg every 8 hr given as a 1 hr infusion for 14-21 days). Treatment for •increased intracranial pressure, •management of seizures, and •respiratory compromise may be required.
  • 29. Infections in Immunocompromised Persons •Severe mucocutaneous and disseminated HSV infections in immunocompromised patients should be treated with intravenous acyclovir (5-10 mg/kg or 250 mg/m2 every 8 hr) until there is evidence of resolution of the infection. •Oral antiviral therapy with acyclovir, famciclovir, or valacyclovir has been used for treatment of less-severe HSV infections and for suppression of recurrences during periods of significant immunosuppression. •Acyclovir-resistant viruses are often also resistant to famciclovir but may be sensitive to foscarnet or cidofovir.
  • 30. PROGNOSIS Most HSV infections are self-limiting, last from a few days (for recurrent infections) to 2-3 wk (for primary infections), and heal without scarring. Recurrent oral-facial herpes in a patient who has undergone dermabrasion or laser resurfacing can be severe and lead to scarring. Lifethreatening conditions include •neonatal herpes •herpes encephalitis •HSV infections in immunocompromised patients •burn patients •severely malnourished infants and children. Recurrent ocular herpes can lead to corneal scarring and blindness.
  • 31. PREVENTION oTransmission of infection occurs through exposure to virus either as the result of skin-to-skin contact or from contact with contaminated secretions. oGood handwashing ouse of gloves oClean shared toys and athletic equipment such as wrestling mats at least daily after use oUse of sun blockers is reported to be effective in preventing orecurrent oral-facial herpes in patients with a history of sun-induced recurrent disease.