Dermatopathology #2 Flashcards
What’s the diagnosis? Note the calcified elastic fibers that look like snipped elastic bands.
Pseudoxanthoma elasticum
What’s the most likely diagnosis?
Pseudoxanthoma elasticum
What’s the diagnosis?
Ichthyosis vulgaris
*Note: usually orthokeratosis is associated with an increased granular layer. Ichthyosis vulgaris is the one exception to this rule.
**Note: usually parakeratosis is associated with an absent granular layer. Granular parakeratosis is the one exception to this rule.
What’s the most likely diagnosis? Note the compact orthokeratosis and greatly reduced granular layer.
Ichthyosis vulgaris
What genodermatosis could be represented in the image below?
Vesicular stage of Bloch-Sulzberger disease (incontinentia pigmenti)
*Note: mutation is in the NEMO gene (leads to defective activation of NF-KB)
What genodermatosis could be represented in the image below?
Incontinentia pigmenti (pigmented stage)
What’s the diagnosis? Note the polka-dot pattern of mastocytes.
Mastocytoma
What’s the diagnosis?
Mastocytoma
What cells are seen below?
Mast cells
What’s the diagnosis? What stain might be used to enhance the characteristic cells?
- Telangiectasia macularis eruptiva perstans (TMEP)
- Leder chloroacetate esterase stain (will stain mast cells even after they’ve degranulated)
*Image: Leder stain in TMEP
True or false: a Giemsa stain can be used to highlight mast cells in TMEP.
True
List a stain, other than a Leder stain or Giemsa stain, that can be used to highlight mast cells.
Toluidine blue; will stain mast cell granules metachromatically (i.e. the stain is blue, but the granules will stain purple)
*Note: this stain requires the presence of mast cell granules (i.e. the mast cells won’t stain if they’ve degranulated)
**Note: toluidine blue will also highlight mucin
In addition to mast cells, what other type of cells will a Leder stain highlight?
Myeloid cells (e.g. in leukemia cutis)
What’s the diagnosis? Note the spindled mast cells (a special stain would be required to identify these as mast cells since their morphology is so abnormal).
Telangiectasia macularis eruptiva perstans (TMEP)
This is a Leder stain. What’s the diagnosis?
Telangiectasia macularis eruptiva perstans
Name this histologic pattern. Note that this histologic pattern can be seen in a variety of conditions, including palmoplantar keratodermas and bullous congenital ichthyosiform erythroderma.
Epidermolytic hyperkeratosis
*Note: often this is seen in a solitary epidermolytic acanthoma (i.e. in addition to palmoplantar keratodermas and bullous congenital ichthyosiform erythroderma)
What are the four clinical (and histologic) variants of pyoderma gangrenosum?
- Ulcerative
- Pustular
- Bullous
- Vegetative
*Note: these are both clinical and histologic variants.
In this tumor there is a platelike growth of keratinocytes that runs parallel to the epidermis, with several points of attachment to the epidermis.
Tumor of the follicular infundibulum (infundibuloma)
True or false: P16 will be lost in melanoma.
True; p16 is a tumor suppressor gene that is often lost in melanoma (especially in some inherited forms of melanoma)
True or false: HMB-45 will be positive in a nevus, but only at the junctional component (it will decrease as the nevus cells mature towards the bottom of the nevus).
True
True or false: HMB-45 will be positive in a blue nevus, all the way down to the bottom of the lesion.
True
True or false: HMB-45 will be positive in melanoma, but negative in the deep parts of a nevus.
True; HMB-45 will be positive in melanoma and the junctional component of nevi, but will be negative in the deep parts of nevi
*Note: HMB-45 will be positive all the way to the bottom of a blue nevus
List four stains that can help you distinguish between a spindled melanoma and a spindled SCC (two stains that will be positive in SCC, but negative in melanoma, and two stains that will be positive in melanoma, but negative in SCC).
- Keratin 5.6 and P63; both of these will be positive in SCC and negative in melanoma
- S100, HMB-45, Melan-A, and MITF will all be positive in melanoma and negative in SCC
What’s the diagnosis?
Lichen sclerosus et atrophicus
*Note the “red, white, and blue sign”, with red hyperkeratosis, white papillary dermal edema, and a blue lymphoid band.
What’s the diagnosis?
Radiation induced dermatitis
*Note: the biopsy looks a lot like lichen sclerosus et atrophicus, but doesn’t have the lymphoid band. Also, adnexal structures are gone, and “radiation fibroblasts” may be seen at higher magnification.
What’s the diagnosis?
Radiation-induced dermatitis
What’s the most likely diagnosis? Note the rectangular biopsy, suggesting that the skin was rock hard.
Morphea
*Note: there are very little white spaces between the collagen fibers.
What’s the most likely diagnosis? Note the “trapped” eccrine coil.
Morphea
What’s the diagnosis?
Morphea
*Note: papillary dermal palor may be seen, like in lichen sclerosus et atrophicus (LSEA), but there is never a lyphoid band in morphea, like there often is in LSEA.
True or false: this biopsy could represent morphea.
True; lymphoplasmocytic infiltrates are common at the dermosubcutaneous junction in morphea
What’s the most likely diagnosis in this biopsy showing decreased CD34 staining?
Morphea
*Note: this is an early finding in morphea.
What’s the most likely diagnosis in this patient with peripheral eosinophila? Note the thickened fascia.
Eosinophilic fasciitis
What’s the diagnosis? Note that at higher magnification altered elastic fibers would be present within the tortuous channel in the epidermis.
Elastosis perforans serpiginosa (EPS)
*Begins in childhood or early adulthood, and 40% of cases are associated with a genetic disorder such as Down’s syndrome, Ehler-Danlos, Marfan’s syndrome, etc.
**Can occur secondary to penicillamine.
What’s the diagnosis? Note that collagen fibers are being eliminated.
Reactive perforating collaginosis (RPC)
*Begins during childhood after superficial trauma (Koebnerization), and usually involves the hands and arms.
**Tends to spontaneously resolve over 6-8 weeks.
What’s the diagnosis?
Scar
*Note: the fibroblasts run East-West, and the blood vessels run North-South
What’s the diagnosis in this previously traumatized skin?
Hypertrophic scar
What’s the diagnosis in this previously traumatized skin?
Keloid scar
What’s the diagnosis in this patient who smokes, and who has an extensive sun-exposure history.
Favre–Racouchot syndrome
*Note: smoking is thought to contribute to this disorder.
What’s the diagnosis in this biopsy of the ear?
Chondrodermatitis nodularis helicis
*Note: this is essentially a small decubitus pressure ulcer of the ear.
**Note: fibrin is typically present at the base of the ulcer, and granulation tissue is typically present adjacent to this.
What’s the diagnosis? What molecule is being deposited?
- Ochronosis
- Homogentisic acid
*Ochronosis is the connective tissue manifestation of alkaptonuria. In this condition, the urine turns a brown colour on exposure to air.
What’s “inherited ochronosis” called? What enzyme is deficient?
- Alkaptonuria
- Homogentisate 1,2-dioxygenase
What’s the diagnosis in this patient with an extensive history of sun exposure? Note the collagen that is beginning to look like amyloid.
Adult colloid milium
This condition occurs secondary to chronic lyme borreliosis. Name the condition and the infectious cause.
*Note: fat and large vessels are found close to the epidermis, due to a decrease in the thickness of the dermis.
- Acrodermatitis chronica atrophicans
- Borrelia afzelii (found in Europe, not America)
What’s the diagnosis in this patient with a chronic lyme borreliosis? Note the fat and eccrine coil that are very high in the biopsy, due to dermal atrophy.
Achrodermatitis chronica atrophicans
What’s the diagnosis in this biopsy from the back? Note the fingers of fat that are extending upwards to surround the adnexal structures.
Scleredema
*Note: mucin is pushing apart the normal collagen fibers (mucin may be removed during processing, but not always).
What’s the diagnosis in this biopsy from the shin? Note the attenuated collagen fibers that have been reduced to fine wisps.
Pretibial myxedema
*Almost always seen with Grave’s disease, but also reported with Hashimoto’s thyroiditis, primary hypothyroidism, and even euthyroidism.
What’s the diagnosis? Note the mucin deposition and fibroblast proliferation.
Scleromyxedema
*Marked proliferation of irregularly arranged fibroblasts, increased collagen, and diffuse deposits of mucin.
**Significance of monoclonal gammopathy is unknown.
What’s the diagnosis in this condition that closely resembles scleromyxedema histologically?
Nephrogenic systemic sclerosis
*Note: occurs in the context of renal failure, especially in patients who have received gadolinium enhanced MRI.
What’s the diagnosis in this biopsy containing mucin and inflammation surrounding the eccrine coil?
Tumid lupus
What condition is histologically indistinguishable from tumid lupus (and may in fact be a variant of tumid lupus)? This condition occur primarily on women’s chests.
Reticulated erythematous mucinosis
What’s the diagnosis? What would the diagnosis be if this biopsy were taken from an acral site?
- Focal mucinosis
- Digital myxoid cyst
What’s the diagnosis in this nodular condition? Note that plasma cells may be prominent in, and around, the nodule.
Nodular amyloidosis
*Note: may occur as a purely cutaneous condition, or in association with a primary systemic amyloidosis.
What’s the diagnosis in this patient with notalgia paresthetica? This biopsy was taken from the back.
Macular amyloidosis
*Note: the amyloid is epidermally derived (from dead keratinocytes that eventually turn into amyloid).
**Note: the amyloid is outlined by a fine network of melanophages.
What’s the diagnosis in this patient with lichen simplex chronicus of the lower leg?
Lichen amyloidosis
*Note: this condition occurs most commonly on the lower legs.
What’s the diagnosis in this patient with renal failure? What other disease is this condition associated with?
- Calciphylaxis
- Hyperparathyroidism
*Note: atherosclerosis will also cause calcification of blood vessels, but usually it’s just the large vessels that are involved.
What material is present in the accumulations of amyloid seen in nodular amyloidosis (i.e. what is deposited to create the amyloid)?
Immunoglobin light chains
What’s the diagnosis? Note that there are no shadow cells.
*Hint: this condition occurs most commonly on the necks or chins of 8-10 year olds. It can also occur on the heel of a newborn after a heel-stick.
Subepidermal calcified nodule
What’s the diagnosis in this scrotal biopsy?
Scrotal calcinosis
*Note: considered to be “idiopathic” by some, but may represent calcifications of epidermoid cysts.
**Note: the scrotum is one of the few places where smooth muscle will be present in the dermis, other than in vessel walls and erector pili muscles. The areola is the other site where this occurs.
What’s the diagnosis?
Gout
What’s the diagnosis? Note that the fissured material may stain with cystal violet, Congo red, and thioflavin, but will not stain with pagoda red.
Colloid milium
*Note: the fissured material is NOT amyloid, although it may stain with some amyloid stains (albeit weakly).
What’s the diagnosis in this patient with a ferrochelatase deficiency?
Erythropoietic protoporphyria
*Note: there’s massive reduplication of the blood vessels in the dermis.
What’s the diagnosis in this patient who does NOT have a ferrochelatase deficiency?
Lipoid proteinosis
*Note: there’s massive reduplication of the basement membrane surrounding blood vessels. This occurs more extensively than in erythropoietic protoporphyria (EPP).
What does anisotrichosis mean? In what condition is this finding seen?
- Variability in the diameter of follicles
- Androgenetic balding
True or false: there’s an increased anagen:telogen ratio in androgenetic alopecia.
False; there’s a decreased anagen:telogen ratio
True or false: in relapsing polychondritis, on DIF there’s “full-house” deposition of IgM, IgG, IgA, and C3 in the perichondrium.
True
True or false: neutrophilic eccrine hidradenitis (NEH) can sometimes occur before the diagnosis of leukemia.
True; usually NEH is associated with cytirabine therapy for AML, but occasionally it can occur before treatment begins. In these cases, it’s thought to represent a paraneoplastic phenomenon.
*Note: an idiopathic form of NEH can also occur in children, on the soles of the feet (idiopathic palmoplantar hidradenitis).
True or false: this likely represents an anagen follicle.
False; this likely represents a telogen follicle.
*Note: there’s trichilemmal keratinization that’s producing a “flame thrower” appearance. Also note the entrance of the sebaceous gland.
True or false: this is likely an anagen follicle.
True
True or false: in a catagen hair, there’s often an accordion-like folding of the outer root sheath, and multiple apoptotic cells.
True
What phase of the hair cycle is this hair in? Note the “flame thrower” appearance of the follicle, produced by the bright red trichilemmal keratinization.
Telogen (this appearance begins to develop during catagen though)
What are fibrous tract remnants?
Fibrous tissue that remains after the follicle moves upward in the skin during catagen and telogen (in anagen, the hair is located deeper in the dermis)
What’s the diagnosis? Note the wedge-shaped scar in the infundibular region of this biopsy (i.e. absence of elastic tissue on this Verhoeff Van Gieson stain).
Lichen planopilaris
*Note: the biopsy below shows a burnt out biopsy of LPP (no follicle visible).
What’s the most likely diagnosis?
Discoid LE
True or false: this could represent lupus panniculitis.
True
*Note the lipomembranous changes in the fat (“frost on a window pane”) which is often seen in lipodermatosclerosis.
What’s the diagnosis? At higher magnification, vacuolar interface dermatitis will be seen, but unlike in lupus, there is a “lymph in every hole”. Note the folliculotropism.
Mycosis fungoides (MF); a “lymph in every hole with folliculotropism” is always MF
True or false: lichen planopilaris (LPP) can produce either an interface dermatitis or a vaculoar interface dermatitis, while discoid LE (DLE) of the scalp can produce only an interface dermatitis.
False; it’s the other way around, where LPP can only produce an interface dermatitis, and DLE can produce either an interface dermatitis or a vacuolar interface dermatitis
What’s the diagnosis in this scalp biopsy, where multiple civatte bodies are all that remain of the hair follicle?
Lichen planopilaris
True or false: “bundling” of hairs into a single follicle is typical of alopecia areata.
False; it’s typical of scarring alopecias
True or false: this DIF is consistent with discoid lupus of the scalp.
False; it’s characteristic of lichen planopilaris, with the cytoid bodies being highlighted by IgM
True or false: “shaggy” linear fibrin is typical of lichen planopilaris on DIF.
True
True or false: this suppurative inflammation could be seen in folliculitis decalvans, acne keloidalis nuchae, or pseudopelade of Brocq.
False; Pseudopelade of Brocq is not suppurative, but folliculitis decalvans and acne keloidalis are
What’s the diagnosis? Note the anisotrichosis.
Androgenetic alopecia