GYNAECOLOGY Flashcards

1
Q

Ovary blood supply

A

Right ovarian vein drains into the IVC. Left drains into the left renal vein. Ovarian artery from the aorta.

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2
Q

Ovary physiology

A

Recruitment of follicules, Day 1-5: folllicular selection, those sized between 5-10mm are recruited, the rest become atretic. Day 5-7 there will be a dominant follicale, 10mm in size. grows around 2mm perday. The follicle will reach roughly 20mm in size prior to ovulation.

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3
Q

Average volume. Ovaries

A

7cc in females 20-39years. in post menopausal medial volume is 1cc. Ovaries found between the iliac vessels form the lateral border of the ovarian fossa where the ovaries lies. MRI provides the most detailed assess of the ovaries.

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4
Q

How to find the ovaries

A

look for the ovarian vein. follow the Ovarian vienw along the anterior surface of the psoas . Ureter Ov are typically located anterior or anteromediaal to the pelvic portion of the uretery.

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5
Q

Lexicon

A

Cyst: fluid containing structure with avascular internal contents that may have differing degrees of internal echoes. a cust can contain solid comp that is tissue r non-tissue, avascular or vascular. A cyst can be physiologic or nonphysiological. Solid or solid appearing: mass or component of a mass that has some echos suggestive of tissue, usually iso or hyperechoic when compared with the echogenicity of the normal ovarian parenchyma. Anechoic fluid: smile fluid. Fluid containing internal echoes: not simple fluid. The follicle is a simple cyst < 3cm in a premenopausal group. Ascites: fluid extending above the uterine fundus beyond the POD. Cul-de-sac fluid. Fontined to the pouch of dough below the uterine fundus or between the uterus and bladder. Papillary projections or nodules. >3mm in height.

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6
Q

Reporting an ovarian lesion

A
  1. Cystic or solid or both. Internal contests echogenicity. Border smooth or irregular, papillary projections 2. Uni lat or bilat 3 size, Max diameter 4. Vascularity: peripheral circumferential, doppler flow vs internal colour doppler. can score this via ORADS. 5. General and extra ovarian findings.
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7
Q

Benign ovarian lesions

A

CORPUS LUTEUM: unilocular cyst with thickened irregular crenelated wall. Prominent vascular flow within the cust wall “ring of fire appearance”. Can contain haemorrhage. usuaing less than 3cm. No papillary projections or mural nodule.

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8
Q

Haemorragic cyst

A

reticular pattern fine intersecting lines representing fibrin strands. Reteaching clot: an avascular echogenic component with angular, straigt or concave margins. Assess with real time movement. Might look jelly-like/mobile. Mx: premenopausal: less than 5cm no follow up required. >5cm but <10cm follow up in 8-12weeks. If persists or enlarges referral to specialist or MRI. Post menopausal: Straight to US specialized, Gynecologist or MRI

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9
Q

OVARIAN ENDOMETRIOUS

A

ground glass, low level internal echoes, cyst usually unilocuular, thick walled homogenous echogenic material consisting with old haemorrgaer. No internal doppler flower can contain a fluid-fluid level. Bilateral ovarian involvement in 30-50%. MRI: t2 shading, T2 dark spot. Black dot. Endometrioma associated neoplasm 1% of women. An ovarian endometrioid ca and clear cell can arise in endometriomas. Polypoid endome;triosis - polypoid masses projecting into the lumen of the endometriome. Decidualisation durial pregnancy can respond to hormonal stimulation in pregnancy. Pute mostly during pregnancy with rapid growth.

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10
Q

OVARIAN DERMOID

A

Mature teratoma: hyperechoic component with acoustic shadowing. Hyperechoic lines and dotes. Tip of the iceberg sign. Fat/fluid level. Floating echogenic spherical structures. White ball. presence of fat on CT or MRI is diagnostic. Bilateral in 20% of cases. Complications rupture, torsion, malignant transformation.

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11
Q

IOTA score

A

B-Features: M-Features: M1 - irregular solid tumor (80% is solid in 2 dimensions) M2 - Presence of ascities. M3 - at least 4 papillary projections. (needs to >3mm); M4 - Irrgular multilocularsolid tumour, maximal diamter >100mm M5 - is very strong blood flow (colour score 4).

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12
Q

ADNEX MODEL OF CLASSIFICATION

A

age, onology center. maximal dimeter of the lesion. max diameter of the larges solid part. more then 10 locules number of paillations. Acoustic shadows present. ascities. Serum Ca-125

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13
Q
A
  • rupture follicle bleeds internally and re-expands
  • homogenous mass with enhanced thru transmission(tumour wont do that)
  • similar to endometrioma
  • lacy fishnet appearance
  • no dopple flow.
  • haemorrhaigic cyst will go away in 1-2 cycles
  • so rpt USS in 6-12 weeks.
  • Endometrioma is homogenous with low level echos

Haemorrhagic ovarian cyst

Dr Rania Adel Anan and Radswiki◉ et al.

Haemorrhagic ovarian cysts (HOCs) usually result from haemorrhage into a corpus luteum or other functional cyst. Radiographic features are variable depending on the age of the haemorrhage. They typically resolve within eight weeks.

Clinical presentation

Patients may present with sudden-onset pelvic pain, pelvic mass, or they may be asymptomatic and the haemorrhagic ovarian cyst is an incidental finding 4. A haemorrhagic or a ruptured ovarian cyst is the most common cause of acute pelvic pain in an afebrile, premenopausal woman presenting to the emergency room 5. They can occur during pregnancy.

Pathology

Haemorrhagic ovarian cysts typically develop as a result of ovulation. Secondary to a hormone response the stromal cells surrounding a maturing Graafian follicle become more vascular, and after the oocyte has been expelled, the Graafian follicle develops into a corpus luteum with a highly vascular and fragile granulosa layer, which ruptures easily, forming a haemorrhagic ovarian cyst 4.

Radiographic features

Ultrasound

Haemorrhagic ovarian cysts can have a variety of appearances depending on the stage of evolution of the blood products and clot.

lace-like reticular echoes or an intracystic solid clot

a fluid-fluid level is possible.

thin wall

clot may adhere to the cyst wall mimicking a nodule, but has no blood flow on Doppler imaging

retracting clot may have sharp or concave borders, mural nodularity does not

posterior acoustic enhancement

may be less noticeable if harmonics or compounding is used

there should not be any internal blood flow

circumferential blood flow in the cyst wall is typical

If there is rupture of a haemorrhagic cyst, other findings may be present.

MRI

Relatively well defined cystic lesion in association with the ovary. Signal characteristics can vary depending on the age of the haemorrhage.

T1: high signal

T2: high signal

“T2 shading” is suggestive of chronic blood products and is more typical of endometrioma

haemorrhage evolves from the centre of the cyst and then extends peripherally (i.e. the centre may show chronic stage of haemorrhage while the periphery is more subacute)

T1 C+ (Gd): no enhancement

Treatment and prognosis

Most haemorrhagic cysts resolve completely within two menstrual cycles (8 weeks).

Cysts with a typical appearance of a haemorrhagic cyst should lead to follow-up ultrasound or MRI imaging in 6-12 weeks if:

the cyst is > 5 cm in diameter if the patient is pre-menopausal
or

any size of a haemorrhagic cyst if the patient is perimenopausal 2

In the postmenopausal patient, surgical evaluation is warranted.

A cystic structure that does not convincingly satisfy the criteria for a benign cyst cannot be considered a cyst and should be evaluated with a short interval follow-up ultrasound or MRI

Differential diagnosis

Differential considerations on ultrasound include:

cystic ovarian neoplasm: the most helpful feature in distinguishing ovarian neoplasms from haemorrhagic cysts are

papillary projections

nodular septae

colour Doppler flow in the cystic structure

endometrioma

typically contains uniform low-level internal echoes with a hypervascular wall on Doppler ultrasound.

more often multiple

on MRI, endometrioma shows high signal in T1 and low signal in T2 (shading sign), although there is overlap in appearance with haemorrhagic cysts

See also

haemorrhagic corpus luteal cyst

Quiz questions

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14
Q
A

Mature cystic ovarian teratoma

  • Typical in young women 20-30.
  • most common ovarian neoplasm in patients younger than 20.
  • Tip of the ice berg sign.
  • cystic mass
  • hyperechoic solid mural nodule - rokitansky nodule/dermoid plug
  • septations in 10%
  • MRI: will be bright on T1 (fat), and will fat suppress (unlike hemorragic cystcs and endometriomas)
  • 1% of dermoids can undergo malignant transformation - to SCC usually.
  • Risk factors are size >10cm and age >50 yo.
  • Gross fat containing ovarian mass on CT.
  • Dot dash pattern = hair in cyst.

Annotated ultrasound images showing the Rrokitansky nodule, echogenic mesh (hair), dense shadowing foci (tip of the iceberg) and focus of possible tooth/ossification which are the characteristic features of an ovarian dermoid cyst.

Case Discussion

A mature cystic teratoma of the ovary is also called a dermoid cyst. This patient presented with a palpable lump per abdomen. The initial ultrasound scan showed the characteristic sonographic features of an ovarian dermoid cyst. CT abdomen was done later which confirmed the findings. This case highlights some of the classic features of an ovarian dermoid cyst viz. Rokitansky nodule, tip of iceberg sign, linear mesh of hair, fat-fluid levels and tooth/ossification within. Usually, ovarian dermoid cysts tend to be not more than 10 cm in size, but in this patient, the cyst was very large, reaching superiorly up to the level of the umbilicus.

Hence, based on the characteristic sonographic features, one can reliably make a diagnosis of ovarian dermoid cyst on ultrasound. When findings are not typical, a CT scan can confirm the diagnosis.

Dr Pir Abdul Ahad Aziz◉ and Assoc Prof Frank Gaillard◉◈ et al.

Ovarian dermoid cyst and mature cystic ovarian teratoma are terms often used interchangeably to refer to the most common ovarian neoplasm. These slow-growing tumours contain elements from multiple germ cell layers and are best assessed with ultrasound.

Terminology

Although they have very similar imaging appearances, the two have a fundamental histological difference: a dermoid is composed only of dermal and epidermal elements (which are both ectodermal in origin), whereas teratomas also comprise mesodermal and endodermal elements.

For the sake of simplicity, both are discussed in this article, as much of the literature combines the two entities.

Epidemiology

Mature cystic teratomas account for ~15% (range 10-20%) of all ovarian neoplasms. They tend to be identified in young women, typically around the age of 30 years 1, and are also the most common ovarian neoplasm in patients younger than 20 years 7.

Clinical presentation

Uncomplicated ovarian dermoid tend to be asymptomatic and are often discovered incidentally. They do, however, predispose to ovarian torsion, and may then present with acute pelvic pain.

Pathology

Mature cystic teratomas are encapsulated tumours with mature tissue or organ components. They are composed of well-differentiated derivations from at least two of the three germ cell layers (i.e. ectoderm, mesoderm, and endoderm). They, therefore, contain developmentally mature skin complete with hair follicles and sweat glands, sometimes luxuriant clumps of long hair, and often pockets of sebum, blood, fat (93%) 10, bone, nails, teeth, eyes, cartilage, and thyroid tissue. Typically their diameter is smaller than 10 cm, and rarely more than 15 cm. Real organoid structures (teeth, fragments of bone) may be present in ~30% of cases.

Location

They are bilateral in 10-15% of cases 1,2.

Variants

struma ovarii tumour: contains thyroid elements, however, sometimes these are separately classified as specialised teratomas of the ovaries

Radiographic features

Plain radiograph

May show calcific and tooth components with the pelvis.

Pelvic ultrasound

Ultrasound is the preferred imaging modality. Typically an ovarian dermoid is seen as a cystic adnexal mass with some mural components. Most lesions are unilocular.

The spectrum of sonographic features includes:

diffusely or partially echogenic mass with posterior sound attenuation owing to sebaceous material and hair within the cyst cavity

an echogenic interface at the edge of mass that obscures deep structures: the tip of the iceberg sign

mural hyperechoic Rokitansky nodule (dermoid plug)

echogenic, shadowing calcific or dental (tooth) components

the presence of fluid-fluid levels 5

multiple thin, echogenic bands caused by the hair in the cyst cavity: the dot-dash pattern (dermoid mesh)

colour Doppler: no internal vascularity

internal vascularity requires further workup to exclude a malignant lesion

intracystic floating balls sign is uncommon but characteristic 9

CT

CT has high sensitivity in the diagnosis of cystic teratomas 6 though it is not routinely recommended for this purpose owing to its ionising radiation.

Typically CT images demonstrate fat (areas with very low Hounsfield values), fat-fluid level, calcification (sometimes dentiform), Rokitansky protuberance, and tufts of hair. The presence of most of the above tissues is diagnostic of ovarian cystic teratomas in 98% of cases 5. Whenever the size exceeds 10 cm or soft tissue plugs and cauliflower appearance with irregular borders are seen, malignant transformation should be suspected 5.

When ruptured, the characteristic hypoattenuating fatty fluid can be found as anti dependant pockets, typically below the right hemidiaphragm, a pathognomonic finding 2. The escaped cyst content also leads to chemical peritonitis and the mesentery may be stranded and the peritoneum thickened, which may mimic peritoneal carcinomatosis 2.

Pelvic MRI

MR evaluation usually tends to be reserved for difficult cases but is exquisitely sensitive to fat components. Both fat suppression techniques and chemical shift artifact can be used to confirm the presence of fat.

Enhancement is also able to identify solid invasive components, and as such can be used to accurately locally stage malignant variants.

Treatment and prognosis

Mature ovarian teratomas are slow-growing (1-2 mm a year) and, therefore, some advocate nonsurgical management. Larger lesions are often surgically removed. Many recommend annual follow-up for lesions <7 cm to monitor growth, beyond which resection is advised.

Complications

Recognised complications include:

ovarian torsion: ~3-16% of ovarian teratomas, in general: considered the most common complication

rupture: ~1-4%

malignant transformation: ~1-2%, usually into squamous cell carcinoma (adults) or rarely into endodermal sinus tumours (paediatrics)

superimposed infection: 1%

autoimmune haemolytic anaemia: <1%

hyperthyroidism (in struma ovarii only)

carcinoid syndrome (rare)

paraneoplastic anti-N-methyl-D-aspartate receptor (anti-NMDA receptor) associated limbic encephalitis (uncommon) 8

Differential diagnosis

General differential imaging considerations include:

haemorrhagic ovarian cyst

endometrioma

a high T1 signal that does not suppress with fat saturation

T2 shading

pedunculated lipoleiomyoma of the uterus

can be traced back to the uterus

immature teratoma

ovarian serous or mucinous cystadenoma/cystadenocarcinoma

this is usually only a serious consideration if typical features of mature cystic teratoma are absent (i.e. fat is absent)

tend to occur in an older age group than dermoid cysts

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15
Q

Most common ovarian malignancy

A
  • Serous ovarian cancer/cystadenocarcinoma/cystadenoma
  • 60% benign
  • 15% borderline
  • 25% malignant - tending to occur in older women
  • women of childbearing age
  • unilocular with few septations
  • Frequently bilateral (esp when malig)
  • Papillary projections are a common finding and are suggestive of malignant
  • ascities = mets
  • 70% have pertioneal involvement at time of diagnosis.
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16
Q

Which type of ovarian ca can cause pseudomyoma pertionei?

A
  • Mucinous ovarian cystadeoncarcinoma
  • often a large mass
  • typically multiloculated (although setpal are often thin
  • Papillary projections are less common than with serous tumours
  • Mucin causes low level echos.
  • Pseudomyxoma peritoneai with scalloping along solid organs
  • smoking is a risk factor
    • Crack the code pg 295

Radiographic features (radiopedia)

In general, the cell type (e.g. serous, mucinous) often cannot be determined by the appearance on imaging 5. While some of the specific features can vary between the subtypes, there are certain features which are more common among mucinous tumours: 3

often larger than their serous counterparts (on occasion they may be enormous)

tend to be more multilocular with small cystic components +/- honeycomb-like locules

calcification is comparatively rare and if present tends to be linear

usually unilateral

peritoneal carcinomatosis is less common compared with serous tumours

may have accompanying pseudomyxoma peritonei

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17
Q

Second most common ovarian cancer

A
  • Endometriod Ovarian cancer (Crack the core pg 295).
  1. serous
  2. endometrioid
  3. Mucinous
  • Bilateral 15% of the time
  • 25% of women will have concomitant endometrial cancer with the endometrial cancer as the primary and ovary as a met
  • Endometrioid carcinoma of the ovary

Dr Bahman Rasuli◉ and Dr Alexandra Stanislavsky◉ et al.

Endometrioid carcinomas of the ovary are a sub-type of epithelial ovarian tumours. The vast majority are malignant and invasive. On imaging, they are usually characterised as complex nonspecific solid-cystic masses and found associated with endometriosis.

Epidemiology

Endometrioid carcinomas account for 8-15% of all ovarian carcinomas. It is considered the second commonest malignant ovarian neoplasm 8.

Both endometrioid and clear cell tumours are frequently associated with endometriosis 9.

Pathology

The typical gross appearance of these tumours is similar to that of other epithelial lesions, with variable cystic and solid components. Occasionally, it may be completely solid.

Histologically, an endometrioid carcinoma is characterised by the appearance of tubular glands and bears a strong resemblance to the endometrium. Gross morphological appearance is that of a mass with both solid and cystic areas 2. Squamous differentiation can be present in more than a third of patients 8.

A benign endometrioid carcinoma is relatively uncommon and when it is benign it tends to be an ovarian cystadenofibroma 3.

Associations

synchronous endometrial carcinoma or endometrial hyperplasia may be present in up to a third of cases

the endometrial abnormality is thought to represent an independent, primary lesion rather than metastatic disease

endometrioid carcinoma is the most common malignant neoplasm arising within an endometrioma, although overall this is an uncommon occurrence

Location - laterality

Bilateral involvement can be seen in 25-40% of cases 1-2,8.

Radiographic features

Imaging findings are often non-specific and include a large, complex cystic mass with solid components.

There may be associated endometrial thickening, evidence of endometriosis or a contralateral mass.

MRI

Reported signal characteristics include:

T2:

relatively low signal intensity of the tumour wall

shading sign may be seen 3

T1 C + (Gd): can show mild enhancement 3

Treatment and prognosis

Endometrioid histology may carry a slightly better prognosis than a serous or mucinous cystadenocarcinoma of the ovary (not a serous tumour in general) independent of stage 5,8. Pure endometrioid tumours carry a far better outcome than a mixed variety.

Differential diagnosis

Metastases to the ovary with colon cancer could be considered especially if the ovarian lesion is bilateral or if there is a known colonic mass, especially due to strong histological similarity. Differentiation from metastatic endometrial cancer can also sometimes be difficult.

See also

ovarian tumours

References

18
Q

differential for BFM (big fucking mass) in an adult

A
  • Adult
    • Ovarian masses (mucinous and serous)
    • Desmoids (Gardner Syndrome)
    • Sarcomas

Gardner syndrome

Dr Francis Deng◉ and Assoc Prof Frank Gaillard◉◈ et al.

Gardner syndrome is one of the polyposis syndromes. It is characterised by:

familial adenopolyposis

multiple osteomas: especially of the mandible, skull, and long bones

epidermal cysts

fibromatoses

desmoid tumours of mesentery and anterior abdominal wall

Other abnormalities include:

supernumerary teeth and odontomas 4

duodenal tumours / ampullary carcinoma 2,3

papillary thyroid carcinoma

Pathology

There is an autosomal dominant inheritance in the FAP gene (chromosome 5q) in a majority of patients but with 20% of cases resulting from new mutations. Extracolonic features often precede the diagnosis of colonic polyps.

History and etymology

First described in 1953 by Gardner and Richards 3.

19
Q

What is Meigs syndrome?

A
  • Triad of ascites
  • pleural effusion
  • benign ovarian tumour (most commonly a fibroma)

Meigs syndrome

Dr Yuranga Weerakkody◉ et al.

Meigs syndrome is defined as the presence of ascites and pleural effusion in association with a benign, usually solid ovarian tumour. In the vast majority (80-90%) of cases, the primary tumour is an ovarian fibroma. Other primary tumours include:

ovarian fibrothecoma

ovarian thecoma

granulosa cell tumours of the ovary

Brenner tumour: rare

Pathology

The pathophysiology of ascites in Meigs syndrome is speculative. It was initially suggested that irritation of the peritoneal surfaces by a hard, solid ovarian tumour could stimulate peritoneal fluid production. The pathophysiology of the pleural effusion is also speculative with some suggesting ascitic fluid being transferred via trans-diaphragmatic lymphatic channels into the pleural space.

Distribution

The pleural fluid tends to be right sided in a majority (~60-70%) of cases.

Treatment and prognosis

The condition is benign and the ascites and pleural effusion resolve after resection of the primary pelvic tumour.

History and etymology

Named after Joe Vincent Meigs (1892-1963), an American (US) obstetrician and gynaecologist 4.

Differential diagnosis

General considerations include:

malignant ascites and pleural effusion in the presence of an aggressive ovarian tumour

pseudo-Meigs syndrome: benign reversible pleural effusion in the presence of a primary tumour other than solid ovarian tumours, e.g. broad ligament leiomyoma

Quiz questions

20
Q

Ovarian Fibroma/fibrothecoma

A
  • ovavrian fibroma is a benign ovarian tumour
  • middle aged women
  • very similar to a fibroid
  • hypoechoic and solid
  • T1 and T2 dark with a band of T2 dark signal around the tour on all planes
  • Calcs are RARE
  • Meigs syndrome
    • fibroma
    • pleural effusion
    • ascites
21
Q

brenner tumour

A
  • epithelial tumour of the ovary seen in women in their 50s-70s.
  • Fibrous
  • T2 dark
  • Unlike fibromas calcs are COMMON (80%)
  • AKA - Ovarian transitional cell carcinoma

Brenner tumour

Dr Bahman Rasuli◉ and Dr Gagandeep Choudhary et al.

Brenner tumours are an uncommon surface epithelial tumour of the ovary. It was originally known as a transitional cell tumour due to its histological similarity to the urothelium. Brenner tumours account for ~3% of ovarian epithelial neoplasms. They can very rarely occur in other locations, including the testis.

Epidemiology

Most often found incidentally in women between their 5th and 7th decades of life.

Clinical presentation

They are most frequently found incidentally on pelvic examination or at laparotomy.

Pathology

Histological specimens often show transitional cells similar to neoplasms of the urothelium 8.

Associations

Brenner tumours are associated with another epithelial ovarian neoplasm of either the ipsilateral or contralateral ovary in ~30% of cases 6.

Location

Brenner tumours can be bilateral in 6-7% of cases.

Radiographic features

Often manifesting as a multilocular cystic mass with a solid component or as a mostly solid mass.

Tumours are usually small (<2 cm). Even with the occasional large tumour (>10 cm), there is often a lack of local invasion, lymphadenopathy, ascites, or metastases (i.e. peritoneal metastases, omental caking), which help distinguish it from other malignant ovarian neoplasms.

Pelvic ultrasound

Brenner tumours are similar to other solid ovarian neoplasms, particularly fibromas-thecomas, and can also be confused with pedunculated leiomyomas.

They are mainly hypoechoic solid masses. Calcifications have been reported in 50% of Brenner tumours on ultrasound.

CT

calcifications have been reported in ~85% of Brenner tumours on CT

solid component may show mild to moderate enhancement post-contrast

MRI

due to its predominantly fibrous content, they appear hypointense on T2-weighted sequences

Treatment and prognosis

Most Brenner tumours are benign.

Differential diagnosis

General imaging differential considerations include:

ovarian fibroma

ovarian fibrothecoma

pedunculated leiomyoma

References

22
Q

ovarian mass and Hyper thyroid

A
  • STUMA OVARII
  • subtype of ovarian teratoma
  • multilocular
  • predominantly cystic mass
  • INTENSELY enhancing solid component
  • MRI GIVEAWAY - the cysts are T2 dark which is usually thick colloid
  • Catain thyroid tissue
23
Q

% of ovarian malig which is metastatic

A
  • 10% of malignant ovarian tyours are mets
  • the primary is most commonly from colon, gastric, breast, lung and contralateral ovary
  • the most common look is bilateral solid tumours
  • KRUKENBURG tumour
    • met to the ovariy from the GIT - usually stomack

Krukenberg tumour (case)

Dr Mohammad Taghi Niknejad and Dr Yuranga Weerakkody◉ et al.

Krukenberg tumour, also known as carcinoma mucocellulare, refers to the “signet ring” subtype of metastatic tumour to the ovary. The colon and stomach are the most common primary tumours to result in ovarian metastases, followed by the breast, lung, and contralateral ovary.

Epidemiology

The tumours represent 5-10% of all ovarian tumours and up to 50% of all metastatic tumours to the ovary. The estimated incidence of Krukenberg tumour is at approximately 0.16/100000 per year. They tend to develop during the reproductive years 4-5.

Clinical presentation

Abdominal or pelvic pain, abdominal bloating, or pain during intercourse, may be the presenting symptom. Irregular bleeding may also be seen.

Median patient age at presentation is 48 years.

Pathology

Krukenberg tumours are metastatic tumours to the ovary that contain well defined histological characteristics - mucin-secreting “signet ring” cells and usually originate in the gastrointestinal tract 4.

The time from diagnosis of the primary neoplasm to the development of ovarian metastasis is variable and can range from several months to >10 years.

Cytologic examination often reveals mucoid degeneration and many large cells shaped like signet rings.

They can originate from 1:

stomach cancer (signet-ring cells): most common

colorectal carcinoma: second most common

breast cancer

lung cancer

contralateral ovarian carcinoma

pancreatic carcinoma

cholangiocarcionoma/gallbladder carcinoma

Radiographic features

Most imaging features are non-specific, consisting of predominantly solid components or a mixture of cystic and solid areas. It is often difficult to differentiate from other ovarian neoplasms 4-5. There are a variety of metastatic carcinomas to the ovary that can mimic primary ovarian tumours 4.

Pelvic ultrasound

These tumours are typically seen sonographically as bilateral, solid ovarian masses, with clear well-defined margins. An irregular hyper-echoic solid pattern and moth-eaten like cyst formation is also considered a characteristic feature.

CT

CT appearances can be indistinguishable from primary ovarian carcinoma 2. Features will favour towards a Krukenberg tumour if a concurrent gastric or colic mural lesion is seen. There is some evidence that tumours originating from the stomach may be denser on contrast-enhanced CT than those originating from the colon 3.

Pelvic MRI

The great majority of Krukenberg tumours are signet-ring cell carcinomas arising in the stomach. Signet-ring cells scatter in the ovarian stroma with abundant collagen formation or marked oedema. Therefore, Krukenberg tumours can occasionally show low or high signal intensity on T2-weighted images 6.

Krukenberg tumours may demonstrate some distinctive findings on MRI, including:

bilateral complex masses with hypo-intense solid components (dense stromal reaction) 4-5

internal hyperintensity (mucin) on T1 and T2 weighted MR images 4

Strong contrast enhancement is usually seen in the solid component or the wall of the intratumoural cyst 6.

Treatment and prognosis

Differentiation between primary and metastatic ovarian carcinoma is of great importance with respect to treatment and prognosis but may be very difficult based upon imaging findings solely.

Median survival

Median overall survival is of the order of approximately 16 months 8. The breakdown by primary tumour location is as follows 8:

gastric: 11 months
colorectal: 21.5 months
breast: 31 months

other (appendix, gallbladder, small intestine, unknown): 19.5 months

Associated factors for poor prognosis and predictors of unfavourable outcome include 8:

univariate analysis

synchronous metastasis

no chemotherapy

ovarian metastasis beyond the pelvis

multivariate analysis

synchronous metastasis

pelvic invasion

ascites

no metastasectomy

History and etymology

It is named after Friedrich E. Krukenberg, German pathologist (1871-1946) who first described them in 1896.

24
Q
A
25
Q

junctional zone thickness in adenomyosis

A

>12 mm

26
Q

most common cancer of vagina

A

squamous cell

27
Q

most common tumor of vagina in children

A

rhabdomyosarcoma

28
Q

met to vagina in anterior wall, upper 1/3

A

from upper Genital tract

29
Q

met to vagina in posterior wall, lower 1/3

A

from GI tract

30
Q

nabothian cysts

A

on cervix; inflammation causing epithelium plugging of mucous glands

31
Q

gartner duct cysts

A

anterior lateral wall of upper vagina; due to incomplete regression of the Wolffian ducts; can cause mass effect on urethra if at level of urterha

32
Q

Bartholin cysts

A

below pubic symphysis; due to obstruction of Bartholin glands (mucin secreting glands)

33
Q

Skene gland cysts

A

cysts in periurethral glands; can cause recurrent UTIs and urethral obstruction

34
Q

simple cyst in premenopausal women

A

follow up if 5-7 cm
surgical eval/MRI if > 7 cm

35
Q

simple cyst in post menopausal women

A

follow up if > 1cm
surgical eval/MRI if > 7 cm

36
Q

malignant degeneration of endometrioma

A

1%
clear cell or endometroid carcinoma

37
Q

malignant degeneration of dermoid ovarian tumors

A

1%
squamous cell carcinoma

38
Q

nuchal lucency:

  • when is it measured?
  • what is abnormal?
A

anechoic area between neck/occiput and skin
9-12 weeks
should be less than 3 mm

39
Q

criteria diagnostic for pregnancy failure

A
  • CRL of 7 mm, with no heart beat
  • mean gestational sac diameter of 25 and no embryo
  • no embryo with heart beat more than 2 weeks after scan that showed a gestation sac without a yolk sac
  • no embyro with heart beat more than 11 days after scan that showed a gestational sac WITH a yolk sac
40
Q

old school guidelines for abnormal pregnancy

A
  • no yolk sac with mean sac diameter > 8mm
  • absent embryo with mean sac diameter > 16 mm
  • no cardiac activity when embryo can be seen on transabdominal US or > 5 mm on transvaginal