Pediatric Lymphadenopathy Flashcards

1
Q

Define lymphadenopathy

A

Lymph nodes that are abnormal in:

  1. Size
  2. Number
  3. Consistency
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2
Q

The history and PE is the most important component of the work-up in a pediatric pt with LAD. What are some important aspects of the history in this pts?

A
  1. Age of pt
  2. Location of node(s)
  3. Onset and duration of enlargement of node(s)
  4. Localized symptoms (cough, headache, sore throat, skin sores or redness, etc.)
  5. Generalized sxs (fever, wt loss, appetite loss, fatigue, arthralgias, pain, night sweats, pruritis)
  6. Travel, meds, dental problems, bites (flea, tick, mosquito), immunizations, high risk behaviors, hx of LAD, exposures (uncooked meats, animals, unpasteurized milk/soft cheeses, symptomatic individuals)
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3
Q

Important components of PE in evaluating a pediatric pt with LAD

A

Vitals: fever? Weight loss?

Size of nodes

Location of nodes

Quality of nodes — firm, matted, soft, fluctuant, etc.

Localized or generalized

Tenderness, erythema, warmth

Distal lesions (inguinal nodes —look for leg lesion)

Spleen/liver size

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4
Q

In evaluating LN size, what is considered to be enlarged?

A

2+ cm

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5
Q

When evaluating the location of LAD, what location is considered abnormal?

A

Supraclavicular

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6
Q

If the quality of the LNs on exam is tender, warm, red, and fluctuant, you should consider _____ in the Ddx

A

Lymphadenitis

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7
Q

Soft, mobile, smooth LNs are considered benign, while firm and rubbery indicate possible _____

A

Lymphoma

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8
Q

Fixed and matted LNs may indicate malignancy or ___

A

TB

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9
Q

Common causes of LAD in children

A

Viral illness —> “shotty” nodes of early childhood (cervical, axillary, inguinal)

Reactive cervical LAD common in preschool/early school age (URI, OM, conjunctivitis)

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10
Q

When it comes to treatment plan for pediatric LAD, the “shotgun” approach is not appropriate. What are your 3 main options?

A
  1. Watchful waiting — if etiology is obvious or if node(s) are not concerning; with or w/o abx therapy
  2. Abx — if bacterial infection in LN itself or the drainage region is suspected
  3. Possible bx
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11
Q

When should you proceed with LN biopsy?

A

If watchful waiting is the plan but nodes never improve

If 4-6 wks of abx fail to improve LAD

Right away if enlarged supraclavicular node is palpated along with findings consistent with malignancy (night sweats, weight loss, abnormal CXR or CT)

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12
Q

Etiologic organism and manifestations of cat scratch disease

A

Bartonella henselae

Isolated adenopathy, visceral organ (liver and spleen) involvement, parinaud’s syndrome and/or neuroretinitis (PE finding of macular star), CNS involvement with encephalopathy, transverse myelitis, radiculitis, cerebellar ataxia

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13
Q

2 categories of tumor-like lesions of infancy and childhood

A
  1. Heterotopic — microscopically normal cells or tissues that are present in abnormal locations; usually insignificant but rarely can become malignant
  2. Hamartoma — excessive, focal overgrowth of cells and tissues native to the organ in which it occurs (hemangiomas, rhabdomyomas of the heart, etc.); benign histology, can cause clinical problems d/t location, size, etc.
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14
Q

Most common tumors of infancy; most commonly affect the skin in children and usually regress with age

A

Hemangioma

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15
Q

Benign lymphatic tumors seen in pediatrics

A

Lymphangiomas (hamartomatous or neoplastic)

Lymphangiectasis

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16
Q

Benign tumors seen in children

A

Hemangiomas

Lymphatic tumors (lymphangiomas, lymphangiectasias)

Fibrous tumors (fibromatosis, fibrosarcoma)

Teratomas (sacrococcygeal most common)

17
Q

The most frequent malignant cancers in childhood arise in what 5 organ systems?

A

Hematopoietic system

Nervous tissue

Soft tissues

Bone

Kidney

18
Q

What malignancies show sharp peaks in incidence in children <10 y/o?

A
Leukemia (mainly ALL)
Neuroblastoma
Wilms tumor
Hepatoblastoma
Retinoblastoma
Rhabdomyosarcoma
Teratoma
Ewing sarcoma
Juvenile astrocytoma
Medulloblastoma
Ependymoma
19
Q

Most common extracranial solid tumor of childhood

A

Neuroblastoma

20
Q

Presentation of neuroblastoma

A

In children <2: fever, large abdominal mass, possible wt loss, “blueberry muffin baby”

Older children: may not be diagnosed until metastatic — bone pain, respiratory sxs, GI complaints, periorbital region (common site of mets)

21
Q

About 90% of neuroblastomas produce catecholamines which produce elevated urine ____ and _____, which are important diagnostic features

A

VMA; HVA

22
Q

Most common primary renal tumor of childhood and 4th most common pediatric malignancy

A

Wilms tumor

23
Q

The risk of wilms tumor is increased with at least 3 recognizable groups of congenital malformations associated with distinct chromosomal loci. These include WAGR syndrome, Denys-Drash syndrome, and ______________. The latter being characterized by enlargement of body organs, macroglossia, hemihypertrophy, omphalocele, abnormal large cells in adrenal cortex, and chromosomal WT2 abnormality

A

Beckwith-Wiedemann syndrome

24
Q

Various presentations of wilms tumor

A

A large abdominal mass

Hematuria

Pain in abdomen after some traumatic incident

Intestinal obstruction

HTN

Pulmonary metastases