Sandbox:Rina Ghorpade: Difference between revisions

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==Clinical Features==
==Clinical Features==
<br />
{| class="wikitable"
|+
!Features
!Port-wine stain
!Salmon patch
!Infantile hemangioma
|-
|Other names
|Nevus flammeus
|
* Navus simplex
* Stroke bite
* Angle kiss
* Macular stain
|Hemangioma
|-
|Pathology
|Capillary malformation
|Capillary malformation
|Vasular tumors
|-
|Color
|
* Pink to dark red
* Non-blanchable
|
* Pink red patches
* Blanchable
|
* Bright red
* Raised plaques
|-
|Distribution
|
* Respects midline
* Occurs on one side of face
|
* Eyelid
* Glabella
* Nape of the nack
* Scalp
* Lips
|Can occur anywhere in the skin, mucous
membrane, or internal organs.
|-
|Age at presentation
|Present at birth
|Present at birth
|Not present at birth, but usually occur
within a few months of life.
|-
|Progression
|
* Do not regress
* Become more darker with age
|
* Regresses within two years of life
* Lesions on the back of the neck may persist
|Proliferation phase followed by involution
|-
|Association
|
* Sturge-Weber syndrome
* Klippel-Trenaunay syndrome
|
* Spinal dysraphism,
* Beckwith-Wiedemann syndrome
|PHACE syndrome


===Neurological manifestations===
 
SWS is characterized by the formation of [[leptomeningeal]] [[capillary-venous malformation]] or [[angioma]], which can cause various neurological symptoms such as [[seizures]], [[stroke]], [[intellectual disabilities]], and behavioral issues.
[P: Posterior fossa brain malformation  
 
H: Hemangiomas
 
A: Arterial abnormalities
 
C: Cardiac anomalies, coarctation of aorta
 
E: Endocrine and eye abnoramlities]
|-
|
|
|
|
|}





Revision as of 22:52, 12 June 2020

Clinical Features


Features Port-wine stain Salmon patch Infantile hemangioma
Other names Nevus flammeus
  • Navus simplex
  • Stroke bite
  • Angle kiss
  • Macular stain
Hemangioma
Pathology Capillary malformation Capillary malformation Vasular tumors
Color
  • Pink to dark red
  • Non-blanchable
  • Pink red patches
  • Blanchable
  • Bright red
  • Raised plaques
Distribution
  • Respects midline
  • Occurs on one side of face
  • Eyelid
  • Glabella
  • Nape of the nack
  • Scalp
  • Lips
Can occur anywhere in the skin, mucous

membrane, or internal organs.

Age at presentation Present at birth Present at birth Not present at birth, but usually occur

within a few months of life.

Progression
  • Do not regress
  • Become more darker with age
  • Regresses within two years of life
  • Lesions on the back of the neck may persist
Proliferation phase followed by involution
Association
  • Sturge-Weber syndrome
  • Klippel-Trenaunay syndrome
  • Spinal dysraphism,
  • Beckwith-Wiedemann syndrome
PHACE syndrome


[P: Posterior fossa brain malformation

H: Hemangiomas

A: Arterial abnormalities

C: Cardiac anomalies, coarctation of aorta

E: Endocrine and eye abnoramlities]







Differentiating [disease name] from other Diseases [Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as: [Differential dx1] [Differential dx2] [Differential dx3]

Epidemiology and Demographics The prevalence of [disease name] is approximately [number or range] per 100,000 individuals worldwide. In [year], the incidence of [disease name] was estimated to be [number or range] cases per 100,000 individuals in [location]. Age Patients of all age groups may develop [disease name]. [Disease name] is more commonly observed among patients aged [age range] years old. [Disease name] is more commonly observed among [elderly patients/young patients/children]. Gender [Disease name] affects men and women equally. [Gender 1] are more commonly affected with [disease name] than [gender 2]. The [gender 1] to [Gender 2] ratio is approximately [number > 1] to 1. Race There is no racial predilection for [disease name]. [Disease name] usually affects individuals of the [race 1] race. [Race 2] individuals are less likely to develop [disease name].


Risk Factors Common risk factors in the development of [disease name] are [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4].


Natural History, Complications and Prognosis


The majority of patients with [disease name] remain asymptomatic for [duration/years]. Early clinical features include [manifestation 1], [manifestation 2], and [manifestation 3]. If left untreated, [#%] of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3]. Common complications of [disease name] include [complication 1], [complication 2], and [complication 3]. Prognosis is generally [excellent/good/poor], and the [1/5/10­year mortality/survival rate] of patients with [disease name] is approximately [#%].


Diagnosis Diagnostic Criteria The diagnosis of [disease name] is made when at least [number] of the following [number] diagnostic criteria are met: [criterion 1] [criterion 2] [criterion 3] [criterion 4] Symptoms [Disease name] is usually asymptomatic. Symptoms of [disease name] may include the following: [symptom 1] [symptom 2] [symptom 3] [symptom 4] [symptom 5] [symptom 6]


Physical Examination Patients with [disease name] usually appear [general appearance]. Physical examination may be remarkable for: [finding 1] [finding 2] [finding 3] [finding 4] [finding 5] [finding 6]

Laboratory Findings There are no specific laboratory findings associated with [disease name]. A [positive/negative] [test name] is diagnostic of [disease name]. An [elevated/reduced] concentration of [serum/blood/urinary/CSF/other] [lab test] is diagnostic of [disease name]. Other laboratory findings consistent with the diagnosis of [disease name] include [abnormal test 1], [abnormal test 2], and [abnormal test 3].


Imaging Findings There are no [imaging study] findings associated with [disease name]. [Imaging study 1] is the imaging modality of choice for [disease name]. On [imaging study 1], [disease name] is characterized by [finding 1], [finding 2], and [finding 3]. [Imaging study 2] may demonstrate [finding 1], [finding 2], and [finding 3]. Other Diagnostic Studies [Disease name] may also be diagnosed using [diagnostic study name]. Findings on [diagnostic study name] include [finding 1], [finding 2], and [finding 3].


Treatment Medical Therapy There is no treatment for [disease name]; the mainstay of therapy is supportive care. The mainstay of therapy for [disease name] is [medical therapy 1] and [medical therapy 2]. [Medical therapy 1] acts by [mechanism of action 1]. Response to [medical therapy 1] can be monitored with [test/physical finding/imaging] every [frequency/duration]. Surgery Surgery is the mainstay of therapy for [disease name]. [Surgical procedure] in conjunction with [chemotherapy/radiation] is the most common approach to the treatment of [disease name]. [Surgical procedure] can only be performed for patients with [disease stage] [disease name].


Prevention


There are no primary preventive measures available for [disease name]. Effective measures for the primary prevention of [disease name] include [measure1], [measure2], and [measure3]. Once diagnosed and successfully treated, patients with [disease name] are followed-up every [duration]. Follow-up testing includes [test 1], [test 2], and [test 3].