Myxoma

{{Short description|Myxoid tumor of primitive connective tissue}}

{{for multi|the atrial subtype|Atrial myxoma|the virus|Myxoma virus}}

{{Redirect-distinguish|Myxomatous|Myxomatosis}}

{{Infobox medical condition (new)

| name = Myxoma

| image = Atrial myxoma high mag.jpg

| caption = Micrograph of an atrial myxoma. H&E stain.

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A myxoma (New Latin from Greek {{Lang|grc-latn|muxa}} 'mucus') is a myxoid tumor of primitive connective tissue.{{DorlandsDict|nine/000954944|Myxoma}} It is most commonly found in the heart (and is the most common primary tumor of the heart in adults) but can also occur in other locations.

Types

Table below:{{Cite journal|last=Satter|first=Elizabeth K.|date=2009|title=Solitary superficial angiomyxoma: an infrequent but distinct soft tissue tumor|url=https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1600-0560.2008.01216.x|journal=Journal of Cutaneous Pathology|language=en|volume=36|issue=s1|pages=56–59|doi=10.1111/j.1600-0560.2008.01216.x|pmid=19187115 |s2cid=1528140 |issn=1600-0560}}

class="wikitable"
Myxoma

!Margin

!Vascular pattern

! Cellularity

! Stroma

! Staining characteristics

! Recurrence rate

! Image (see Histology)

Cutaneous myxoma or Superficial angiomyxoma

|Poor to moderately circumscribed, multilobular

|Scattered thin-walled vessels

|Moderately cellular, bland spindled and stellate cells, variable inflammatory cell infiltrate

|Abundant mucin with clefts. Up to 30% have an associated epithelial component

|Vimentin; variable staining with CD34, factor XIIIA, SMA{{ref|1|1}}, MSA{{ref|2|2}} and S-100

|20–30%

|Image:CutaneousMyxoma.jpg

Intramuscular myxoma

|Poorly circumscribed merges with surrounding muscle

|Hypovascular variant; hypervascular variant

|Hypocellular variant; hypercellular variant; bland spindle cells

|Abundant mucin with cystic spaces. Hypercellular variant has strands of collagen

|Vimentin; variable staining with actin, desmin, CD34

|None

|Image:IntramuscularMyxoma.JPG

Juxta-articular myxoma

|Poorly circumscribed infiltrates surrounding tissue

|Focally vascular

|Focally hypercellular, peripheral spindle cells with occasional atypical cells and mitoses

|Abundant mucin, 89% of cases contain cystic spaces lined by fibrin or collagen

|Vimentin; variable staining with actin, desmin, CD34

|34%

Aggressive angiomyxoma

|Infiltrative

|Uniformly distributed medium-sized blood vessels often with prominent hyalinization

|Low to moderately cellular, evenly distributed round, spindled or stellate cells

|Loose myxoid to focally collagenous

|Vimentin, desmin, SMA{{ref|1|1}}, MSA{{ref|2|2}}, estrogen and progesterone receptor

|36–72%

Angiomyofibroblastoma

|Well circumscribed

|Abundant thin-walled blood vessels

|Alternating hypercellular and hypocellular areas, perivascular condensations of spindled to epithelioid stromal cells

|Collagenous to edematous with minimal mucin

|Vimentin, desmin, CD34, estrogen and progesterone receptor

|No recurrences reported, but rare cases of sarcomatous degeneration

Superficial acral fibromyxoma

|Pushing to infiltrative

|Mild to moderately accentuated vasculature

|Moderately cellular, spindle and stellate cells with a storiform to fascicular pattern, variable mast cells

|Myxoid to collagenous

|CD34, EMA{{clarify|date=July 2012}}{{ref|3|3}}, CD99

|Recurrence rare and primarily for incompletely excised lesions

Neurothekeoma (Nerve sheath myxoma)

|Well circumscribed, multilobular

|Hypovascular

|Moderately cellular, spindled cells in fascicles and whorls

|Nests of cells separated by collagenous bundles

|S-100, EMA{{ref|3|3}}

|47% if incompletely excised

|Image:Neurothekeoma2.JPG

1.{{note|1}}SMA, smooth muscle actin. 2.{{note|2}}MSA, muscle-specific actin. 3.{{note|3}}EMA, epithelial membrane antigen.

Symptoms and signs

Symptoms associated with cardiac myxomas are typically due to the effect of the mass of the tumor obstructing the normal flow of blood within the chambers of the heart. Because pedunculated myxomas are somewhat mobile, symptoms may only occur when the patient is in a particular position.

Some symptoms of myxoma may be associated with the release of interleukin 6 (IL-6) by the myxoma.{{cite journal |vauthors=Seino Y, Ikeda U, Shimada K | title=Increased expression of interleukin 6 mRNA in cardiac myxomas | journal=Br Heart J | year=1993 | volume=69 | issue=6 | pages=565–7 | pmid=8343326 | doi=10.1136/hrt.69.6.565 | pmc=1025174}}{{cite journal |vauthors=Jourdan M, Bataille R, Seguin J, Zhang XG, Chaptal PA, Klein B | title=Constitutive production of interleukin-6 and immunologic features in cardiac myxomas| journal=Arthritis Rheum | year=1990 | volume=33 | issue=3 | pages=398–402 | pmid=1690543 | doi=10.1002/art.1780330313| doi-access= }} High levels of IL-6 may be associated with a higher risk of embolism of the myxoma.{{cite journal |author1=Wada A |author2=Kanda t |author3=Hayashi R | title=Cardiac myxoma metastasized to the brain: potential role of endogenous interleukin-6 | journal=Cardiology | year=1993 | volume=83 | issue=3 | pages=208–11 | pmid=8281536 | doi=10.1159/000015180|s2cid=22543670 |display-authors=etal}}

Symptoms of a cardiac myxoma include:{{cite journal | author=Fisher J. | title=Cardiac myxoma | journal=Cardiovasc Rev Rep | year=1983 | issue=4 | pages=1195–9}}

Location

File:Myxoma CMR.gif of the heart, showing a large myxoma plunging to and fro from atrium to ventricle across the mitral valve.]]

= Ocular myxoma =

Myxoma is a rare, benign stromal tumor of mesenchymal origin often confused with other conjunctival stromal tumors. Conjunctival myxomas are thought to originate in Tenon's capsule and can masquerade as conjunctival lymphoma, lymphangioma, ocular surface squamous neoplasia (OSSN), or amelanotic melanoma.{{Cite journal|last1=Jain|first1=Puneet|last2=Finger|first2=Paul T|last3=Iacob|first3=Codrin E|date=2018-11-01|title=Conjunctival myxoma: A case report with unique high frequency ultrasound (UBM) findings|journal=Indian Journal of Ophthalmology|language=en|volume=66|issue=11|pages=1629–1631|doi=10.4103/ijo.IJO_518_18|pmid=30355886|pmc=6213696 |doi-access=free }}

File:Myxoma.jpg

= Atrial myxoma =

Myxomas are usually located in either the left or right atrium of the heart; about 86 percent occur in the left atrium.{{cite journal |vauthors=Knepper LE, Biller J, Adams HP, Bruno A |title=Neurologic manifestations of atrial myxoma. A 12-year experience and review |journal=Stroke |volume=19 |issue=11 |pages=1435–40 |year=1988 |pmid=3188128 |doi=10.1161/01.str.19.11.1435|doi-access=free }}

Myxomas are typically pedunculated, with a stalk that is attached to the interatrial septum. The most common location for attachment of the stalk is the fossa ovalis region of the interatrial septum.{{Cite book|last1= Cheng|first1=Davy C.H.|last2=Martin|first2=Janet|last3=David|first3=Tirone|title=Evidence-Based Practice in Perioperative Cardiac Anesthesia and Surgery|date=2020|publisher=Springer Nature|isbn=9783030478872|page=210|url=https://books.google.com/books?id=-44HEAAAQBAJ&pg=PA210}}

An atrial myxoma may create an extra heart sound, audible to auscultation just after S2. It is most seen on echocardiography, as a pedunculated mass that is heterogeneous in appearance. A left atrial myxoma will cause an increase in pulmonary capillary wedge pressure.{{cn|date=November 2021}}

The differential diagnosis include other cardiac tumors such as lipomas and rhabdomyomas (and rarely teratomas). These other tumors of the heart are typically not pedunculated, however, and are more likely to infiltrate the muscle of the heart. Cardiac magnetic resonance imaging (MRI) can help non-invasively diagnose cardiac tumors. However, diagnosis usually requires examination of a tissue sample by a pathologist.{{cn|date=November 2021}}

{{clear}}

Treatment

Myxomas are usually removed surgically. The surgeon removes the myxoma, along with at least 5 surrounding millimeters of atrial septum. The septum is then repaired, using material from the pericardium.{{cn|date=November 2021}}

Epidemiology

Cardiac myxomas predominantly appear in females in their 30s to 40s. Myxomas are the most common primary cardiac tumor affecting adults, accounting for one quarter to half of primary cardiac tumors seen in clinical practice.{{cite journal |last1=Takahashi |first1=Ayaka|display-authors=etal|date=May 2016|title=Multimodal Cardiovascular Imaging of Cardiac Tumors |journal=Annals of Nuclear Cardiology |volume=2 |issue= 1|pages=61–67 |doi=10.17996/anc.2.1_61 |doi-access=free }}

See also

References

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