Hemangioma pathophysiology: Difference between revisions
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*[[POEMS syndrome]] | *[[POEMS syndrome]] | ||
*[[Castleman disease]] | *[[Castleman disease]] | ||
*[[PHACES syndrome]] | |||
==Gross Pathology== | ==Gross Pathology== | ||
*Grossly hemangiomas are described as “spongy” with vascular compartments of various sizes separated by fibrous tissue.<ref name="PapafragkakisMoehlen2011">{{cite journal|last1=Papafragkakis|first1=Haris|last2=Moehlen|first2=Martin|last3=Garcia-Buitrago|first3=Monica T.|last4=Madrazo|first4=Beatrice|last5=Island|first5=Eddie|last6=Martin|first6=Paul|title=A Case of a Ruptured Sclerosing Liver Hemangioma|journal=International Journal of Hepatology|volume=2011|year=2011|pages=1–5|issn=2090-3456|doi=10.4061/2011/942360}}</ref> | *Grossly hemangiomas are described as “spongy” with vascular compartments of various sizes separated by fibrous tissue.<ref name="PapafragkakisMoehlen2011">{{cite journal|last1=Papafragkakis|first1=Haris|last2=Moehlen|first2=Martin|last3=Garcia-Buitrago|first3=Monica T.|last4=Madrazo|first4=Beatrice|last5=Island|first5=Eddie|last6=Martin|first6=Paul|title=A Case of a Ruptured Sclerosing Liver Hemangioma|journal=International Journal of Hepatology|volume=2011|year=2011|pages=1–5|issn=2090-3456|doi=10.4061/2011/942360}}</ref> |
Revision as of 16:27, 18 November 2015
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Nawal Muazam M.D.[2]
Overview
Development of hemangioma is the result of genetic mutations, overexpression of angiogenic fators and downregulation of inhibitors of angiogenesis.[1] Hemangioma may be associated with POEMS syndrome and Castleman disease. On gross pathology, spongy with vascular compartments of various sizes separated by fibrous tissue are findings of hemangioma.[1] On microscopic histopathological analysis, channels lined by benign endothelium containing red blood cells are findings of hemangioma.[2]
Pathophysiology
Pathogenesis
The pathogenesis of hemangiomas has not been elucidated, but there are two competing theories.
First theory
- The first theory supports the notion that there is overexpression of angiogenic factors such as:[1]
- And there is downregulation of some inhibitors of angiogenesis such as:[1]
Second theory
- The second theory is that the presence of liver hemangiomas involves a genetic background of mutations.[1]
- Genetic errors in growth factor receptors have also been shown to affect development of hemangiomas.
- Metalloproteinases can accumulate in the endoplasmic reticulum of the tumor cells causing:
- Self-digestion
- Vacuole formation
- Cavernous hemangioma cell can downregulate Derlin-1.
- Derlin-1 is a protein that when overexpressed induces the dilated endoplasmic reticulum to return to its normal size.
Third theory
- The third theory suggests that hemangioma endothelial cells arise from disrupted placental tissue imbedded in fetal soft tissues during gestation or birth.[3]
- Markers of hemangiomas have been shown to coincide with those found in placental tissue.
- This is further supported by the fact that they are found more commonly in infants following:[3]
Associated Conditions
Hemangioma may be associated with:
Gross Pathology
- Grossly hemangiomas are described as “spongy” with vascular compartments of various sizes separated by fibrous tissue.[1]
- Thrombi may be present and are well separated from the normal liver parenchyma despite the absence of a fibrous capsule.
Microscopic Pathology
On microscopic histopathological analysis channels lined by benign endothelium containing red blood cells are findings of hemangioma.[2]
Gallery
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Intermediate magnification micrograph of a capillary hemangioma. H&E stain.[2]
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Very high magnification micrograph of a capillary hemangioma. H&E stain.[2]
-
Histopathological image representing a cavernous hemangioma of the liver. Surgical excision of the lesion for the impending risk for rupture. H&E stain.[2]
-
Histopathological image reprsenting a cavernous hemangioma of the liver. H&E stain.[2]
Immunohistochemistry
Hemangioma is demonstrated by positivity to:[2]
- CD31 positive
- D2-40 negative
References
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 Papafragkakis, Haris; Moehlen, Martin; Garcia-Buitrago, Monica T.; Madrazo, Beatrice; Island, Eddie; Martin, Paul (2011). "A Case of a Ruptured Sclerosing Liver Hemangioma". International Journal of Hepatology. 2011: 1–5. doi:10.4061/2011/942360. ISSN 2090-3456.
- ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 Microscopic features of hemangioma. Librepathology (2015). http://librepathology.org/wiki/index.php/Hemangioma. Accessed on November 12, 2015
- ↑ 3.0 3.1 Richter, Gresham T.; Friedman, Adva B. (2012). "Hemangiomas and Vascular Malformations: Current Theory and Management". International Journal of Pediatrics. 2012: 1–10. doi:10.1155/2012/645678. ISSN 1687-9740.