21 - 129 - GRAFT-VS-HOST DISEASE Flashcards
most important risk factor for chronic GVHD
history of acute GVHD
The most common presentation of acute GVHD begins with
erythematous-dusky macules and papules of the volar and plantar surfaces and ears that may rapidly become a diffuse morbilliform exanthem
These are diagnostic clinical features of chronic GVHD except?
a. poikiloderma
b. lichen planus-like eruption
c. lichen striatus-like eruption
d. morphea-like features
e. none of the above
c. lichen striatus-like eruption
hese are major risk factors for the development of GVHD except?
a. Female recipient/male donor
b. Unrelated donor
c. Donor leukocyte infusion
d. Stem cell source
A (female donor/male recipient)
These are distinctive clinical features of chronic GVHD except?
a. Depigmentation
b. Papulosquamous lesions
c. Pterygium
d. Scaling
e. None of the above
E
Which statement correctly describes the histopathology of acute GVHD?
a. sparse lymphocytic infiltrates
b. sclerosis of upper dermis
c. atrophy of epidermis
d. follicular plugging
A
Which stage of GVHD is characterized clinically by lesions in >50% BSA, subepidermal clefting histologically, with bilirubin levels of 6 to 14.9 mg/dL?
A. Stage 1
B. Stage 2
C. Stage 3
D. Stage 4
C
Risk factors for chronic GVHD
- history of acute GVHD - most important RF
- human leukocyte antigen incompatibility,
- older age,
- female DONOR/male RECIPIENT,
- peripheral blood stem cell source (vs bone marrow)
first line in the treatment of moderate to severe chronic GVHD
Systemic steroids
in this type of transplantation, the patient’s own Hematopoietic stem cell are returned to the patient following preparative chemotherapy with or without radiation
autologous transplantation
transfer of hematopoietic stem cell (HCs) from a related (nonidentical) or unrelated donor to a recipient
Allogeneic HCT (allo-HCT)
transfer of HCs between identical twins
Syngeneic transplantation
primary cause of non–relapse-related morbidity and mortality in alloHCT, and also rarely occurs following transplantation of solid organs, transfusion of blood products, and autologous transplantation
Graftversus-host disease (GVHD)
the single most important predictor of GVHD
degree of human leukocyte antigen (HLA) mismatch between donor and recipient
organs most commonly associated with acute GVHD
- Skin - 81%
- GI - 54%
- Liver - 50%
Skin involvement is often the first indicator of acute GVHD (81%), followed by GI (54%) and liver disease (50%)
What are the 3 proposed basic requirements for GVHD according to Billingham?
(a) immunocompetent transplanted cells,
(b) host antigens recognizable by the transplanted cells and lacking in the donor, and
(c) a host incapable of mounting an immune response to the transplanted cells
The use of particular chemotherapeutic agents such as ____________ may render the differential diagnosis of toxic erythema of chemotherapy more likely.
Cytarabine
predisposition to these areas may help distinguish new onset acute GVHD from other morbilliform eruptions,
predisposition for acral and perifollicular sites
although these features are not always present.
What are the diagnostic clinical features of Chronic GVHD
■ Poikiloderma
■ Lichen sclerosus–like lesions
■ Lichen planus–like eruption
■ Morphea-like lesions
■ Sclerotic features
What clinical features are seen in both acute and chronic GVHD
■ Erythema
■ Maculopapular rash
■ Pruritus
commonly affected organs in acute GVHD
skin, GI tract, liver
typically presenting with skin rash, new-onset elevation of total bilirubin, and/or voluminous diarrhea
most frequently affected sites in chronic GVHD
skin and nails, oral mucosa, eyes, liver, lungs, and marrow (usually thrombocytopenia)
econd only to skin involvement in frequency in chronic GVHD
Mucosal disease
Erythema, lichen planus–like changes with Wickham striae, erosions and ulcerations, and mucoceles are the most common manifestations
most commonly affected mucosa in chronic GVHD
buccal mucosa
followed by the lips, tongue, and soft palate
histopathologic hallmark feature of acute GVHD
presence of necrotic keratinocytes accompanied by a dermal lymphocytic infiltrate (usually sparse) and basal vacuolar interface alteration