LUT- URETERS- CONGENITALANOMALIES/ INFLAMMATION/ TUMORS Flashcards

1
Q

Congenital anomalies of the ureters are found in about 2% or 3% of all autopsies.

Although
most have little clinical significance, certain anomalies may contribute to obstruction to the flow
of urine and thus cause clinical disease
.

Anomalies of the ureterovesical junction that potentiate
reflux are discussed with pyelonephritis in Chapter 20 .

A
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2
Q

Ureter Congenital Anomalies

A
  1. Dobule and bifid ureters
  2. uretopelvic junction obstruction
  3. Diverticula
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3
Q

Double and bifid ureters .

____________ are almost invariably associated either with totally distinct double renal pelves or with the anomalous development of a large kidney having a
partially bifid pelvis terminating in separate ureters.

A

Double ureter

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4
Q

________________, a congenital disorder, results in hydronephrosis.

It usually presents in infants or children, much more commonly in boys.

However, it is bilateral in
20% of cases and may be associated with other congenital anomalies

A

Ureteropelvic junction (UPJ) obstruction

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5
Q

. It is the most common
cause of hydronephrosis in infants and children.

In adults, UPJ obstruction is more common in
women and is most often unilateral. The condition has been ascribed to abnormal organization
of smooth muscle bundles at the UPJ, to excess stromal deposition of collagen between smooth
muscle bundles, or rarely to congenitally extrinsic compression by polar renal vessels.

There is
agenesis of the kidney on the opposite side in a significant number of cases, probably resulting
from obstructive lesions in utero.

A

UPJ

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6
Q

__________________ are uncommon lesions that are usually
asymptomatic
andare found on imaging studies.

They appear as congenital or acquired
defects and are of importance as pockets of stasis and s

. Dilation
(hydroureter), elongation, and tortuosity of the ureters may occur as congenital anomalies or as
acquired defects.

A

Diverticula, saccular outpouchings of the ureteral wall,

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7
Q

Ureteritis, though associated with inflammation, is typically not associated with infection and is of
little clinical consequence.

A

Ureteritis,

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8
Q

Morphology. The accumulation or aggregation of lymphocytes forming germinal centers in
the subepithelial region may cause slight elevations of the mucosa and produce a fine
granular mucosal surface
_____________

A

** (ureteritis follicularis).**

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9
Q

At other times the mucosa may become
sprinkled with fine cysts varying in diameter from 1 to 5 mm lined by** flattened urothelium**
____________________

A

(ureteritis cystica)

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10
Q

TUMORS AND TUMOR-LIKE LESIONS
Primary tumors of the ureter are rare.

  • *Small benign tumors** of the ureter are generally of
  • *____________**
A

mesenchymal origin.

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11
Q

_____________-is a tumor-like lesion that grossly presents as a small
mass projecting into the lumen, often in children.

The lesion occurs more commonly in the
ureters but may also appear in the bladder, renal pelves, and urethra.

A

Fibroepithelial polyp

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12
Q

Fibroepithelial polyp is composed
of a__________________mass lying beneath the mucosa.

A

loose, vascularized connective tissue

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13
Q

Primary malignant tumors of the ureter resemble those arising in the _____________
The majority are urothelial carcinomas ( Fig. 21-2 ). They are found most frequently
during the sixth and seventh decades of life and cause obstruction of the ureteral lumen.

They
are sometimes multiple and commonly occur concurrently with similar neoplasms in the bladder
or renal pelvis

A

renal pelvis, calyces, and
bladder.

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14
Q

A great variety of pathologic lesions may obstruct the ureters and give rise to hydroureter, hydronephrosis, and sometimes pyelonephritis ( Chapter 20 )

A
  • hydroureter,
  • hydronephrosis,
  • and sometimes pyelonephritis (
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15
Q

. It is not the ureteral dilation that
is of significance in these cases
, but theconsequent involvement of the kidneys.

A
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16
Q

The more
important causes, divided into those of intrinsic or extrinsic origin, are listed in Table 21-1 .
________________ typically results from proximal causes,

A

Unilateral obstruction

17
Q

whereas ______________arises
from distal causes, such as nodular hyperplasia of the prostate. Only sclerosing retroperitoneal
fibrosis is discussed further.

A

bilateral obstruction

18
Q

Major Causes of Ureteral Obstruction

Type of
Obstruction Cause

A
  1. INTRINSIC
  2. EXTRINSIC
19
Q

INTRINSIC TYPE OF OBSTRUCTION

A
  1. CAlculi
  2. Strictures
  3. Tumors
  4. Blood clots
  5. Neurogenic
20
Q

EXTRINSIC

A
  1. Pregnancy
  2. Periureteral Inflammation
  3. Endometriosis
  4. Tumors
21
Q
  • Of renal origin, rarely more than 5 mm in diameter
  • Larger renal stones cannot enter ureters
  • Impact at loci of ureteral narrowing—ureteropelvic junction, where ureters cross iliac vessels, and where they enter bladder—and cause excruciating “renal colic”
A

Calculi

22
Q

Which part among of the ureteral narrowing cause excruciating “ renal coli”

A

UPJ

23
Q

Congenital or acquired (inflammations)

A

Strictures

24
Q

Transitional cell carcinomas arising in ureters
Rarely, benign tumors or fibroepithelial polyps

A

Tumors

25
Q

Congenital or acquired (inflammations)

A

Strictures

26
Q

Massive hematuria from renal calculi, tumors, or papillary necrosis

A

Blood Clots

27
Q

_____________ Interruption of the neural pathways to the bladder

A

Neurogenic

28
Q

________________- Physiologic relaxation of smooth muscle or pressure on ureters at pelvic brim from
enlarging fundus

A

Pregnancy

29
Q

Salpingitis, diverticulitis, peritonitis, sclerosing retroperitoneal fibrosis

A

Periureteral
inflammation

30
Q

Cancers of the rectum, bladder, prostate, ovaries, uterus, cervix; lymphomas,
sarcomas

A

Tumors

31
Q

This refers to an uncommon cause of ureteral narrowing or obstruction characterized by a
fibrous proliferative inflammatory
processencasing the retroperitoneal structures and causing
hydronephrosis
. [1]

The disorder occurs in middle to late age.

A

Sclerosing Retroperitoneal Fibrosis.

32
Q

In some cases , what are the specific causes of Sclerosing Retorperitoneal Fibrosis?

A

In some cases specific causes
can be identified, such as:

  • drugs (ergot derivatives, β-adrenergic blockers),
  • adjacent inflammatory conditions (vasculitis, diverticulitis, Crohn disease),
  • or malignant disease (lymphomas, urinary tract carcinomas).
33
Q

How many percent is Sclerosing Retroperintoneal Fibrosis__________ of cases have no obvious cause and are
considered primary or idiopathic (Ormond disease).

NOTE : Several cases have been reported with
similar fibrotic changes in other sites (such as mediastinal fibrosis, sclerosing cholangitis, and
Riedel fibrosing thyroiditis), suggesting that the disorder is systemic in distribution but
preferentially involves the retroperitoneum. Thus, an autoimmune reaction, sometimes triggered
by drugs, has been proposed as the immediate cause of the systemic disease

A

70%

34
Q
A