Difference between revisions of "Dermatologic neoplasms"
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*[http://www.jci.org/articles/view/24826/figure/2 CTCL (jci.org)]. | *[http://www.jci.org/articles/view/24826/figure/2 CTCL (jci.org)]. | ||
*[http://www.mdconsult.com/das/book/body/199872830-2/0/1709/I4-u1.0-B978-0-443-06694-8..50117-2--f2.fig CTCL (mdconsult.com)]. | *[http://www.mdconsult.com/das/book/body/199872830-2/0/1709/I4-u1.0-B978-0-443-06694-8..50117-2--f2.fig CTCL (mdconsult.com)]. | ||
===IHC=== | |||
Features: | |||
*CD4 +ve.<ref>{{Ref PBoD8|1185}}</ref> | |||
==Merkel cell carcinoma== | ==Merkel cell carcinoma== |
Revision as of 01:31, 21 March 2011
This article deals with dermatologic neoplasms. It includes dermatologic cancer, which can be deadly. Collectively, dermatologic cancers are the most common form of cancer.
Squamous cell carcinoma
Main article: Squamous carcinoma
General
Precursor:[1]
- Actinic keratosis (solar keratosis).
- Clinical: yellow-brown scaly, patches, sandpaper sensation.
Risk factors:[1]
- Sun exposure.
- Immune suppression (e.g. organ transplant recepients).
Notes:
- Keratocathoma - see non-malignant skin disease.
- Some don't believe this entity exists.
- These people sign this entity as low grade squamous cell carcinoma, keratoacanthoma type.[2]
- Some don't believe this entity exists.
Microscopic
Basal cell carcinoma
General
- Very common.
- Sun exposed skin.
- Very rarely metastasizes - so rare... some don't think this is really a malignancy.
Clinical
- Telangiectasias.
- Raised pearly nodule.
As part of a syndrome
- Nevoid basal cell carcinoma syndrome (NBCCS), AKA Gorlin syndrome.
- Bazex syndrome (X-linked).[3]
Microscopic
Features:[4]
- Nest of hyperchromatic (i.e. blue) cells (similar in appearance to basal cells) with:
- Palisading of cells at the edge of the cell nests.
- Artefactual separation of cells (forming the nests) from the underlying stroma.
Notes:
- Palisading = the long axes of the cells are alined and the axes are perpendicular to the interface between the (basaloid cell) nests and stroma.
- There are various subtypes: http://www.pathconsultddx.com/pathCon/diagnosis?pii=S1559-8675%2806%2970110-3.
DDx:
- Trichoepithelioma - no artefactual cleft.[4]
Melanoma
General
- AKA Malignant melanoma.
- Main DDx: melanocytic lesions - especially if pigmented.
- Known as the great mimicker in pathology; it may look like many things.
Clinical
- ABCD = asymmetric, borders (irregular), colour (black), diameter (large).
Microscopic
Features:
- Classic appearance of melanoma:
- Loosely cohesive; mix of small nests of cells, single cells.
- Mixed of spindle and ovoid cell morphology.
- +/-Occasional large binucleated cells.
- Cytoplasm: brown pigment (melanin).
- Prominent (large) red nucleoli (like in serous carcinoma of the ovary).
- Marked nuclear pleomorphism - variation in cell size, shape & staining (like in serous carcinoma of the ovary).
- Nuclear pseudoinclusions (like in papillary thyroid carcinoma).
Notes:
- Can look almost like anything.
- Like it is said that sarcoidosis is in every internal medicine DDx... melanoma is every pathologic DDx.
- Melanomas with:
- An epitheloid cell morphology may mimic adenocarcinoma.
- A spindle cell morphology may mimic spindle cell carcinoma (squamous cell carcinoma) or a sarcoma.
Electron microscopy
- Melanosomes.
Image(s):
Stains
- Fontana-Masson stain, stains melanin.[5]
- May be useful to differentiate melanin from other brown stuff (e.g. lipofuscin, hemosiderin).
IHC
Standard panel:
- S-100 +ve.
- HMB-45 +ve.
- Melan A (MART-1) +ve.
Others:
- SOX10 +ve -- useful for diff. from excision scar.[6]
- SOX-10 = pan-schwannian and melanocytic marker.
Notes:
- The standard panel above (S-100, HMB-45, MART-1) is also positive in other lesions, e.g. cellular blue nevus.
Dermatofibrosarcoma protuberans
- Abbreviated DFSP.
General
- Dermal location.
- Destroys adnexal structures.
Treatment:[7]
- Wide excision.
- May include imatinib (Gleevec).
Microscopic
Features:[7]
- Dermal spindle cell lesion with storiform pattern.
- Spokes of the wheel-pattern.
- Contains adipose tissue within the tumour -- key feature.
- Described as "honeycomb pattern" and "Swiss cheese pattern".
Notes:
- Adnexal structure within tumour are preserved -- this is unusual for a malignant tumour.
DDx:
- Dermatofibroma - has entrapment of collagen bundles at the edge of the lesion.
IHC
Panel:[8]
- CD34 +ve.
- Factor XIIIa -ve.
- S100 -ve (screen for melanoma).
- Caldesmin -ve (screen for muscle differentiation).
- Beta-catenin. (???)
- MIB-1 (proliferation marker).
- Should not be confused with MIB1 a gene that regulates apoptosis.
Cutaneous B-cell lymphoma
- Abbreviated CBCL.
General
- CBCL is less common than cutaneous T-cell lymphoma (CTCL).[11]
Microscopic
Features:
- Dermal lymphoid infiltrate.
- "Grenz zone" - space between the epidermis and the dermal infiltrate - key feature.
IHC
- B cell and T cell markers.
Cutaneous T-cell lymphoma
- Abbreviated CTCL.
General
- Mycosis fungoides - is a subtype (???).
- CTCL is more common than cutaneous B-cell lymphoma (CBCL).[12][13]
Microscopic
- Atypical lymphocytes:
- Have folded "cerebriform" nuclei; Sezary-Lutzner cells.[14]
- Grouping:
Images:
IHC
Features:
- CD4 +ve.[16]
Merkel cell carcinoma
General
Features:[17]
- Rare.
- Aggressive course/poor prognosis.
- Neuroendocrine-like.[18]
Etiology:
- Polyomavirus (?).[17]
- Immunocompromised/immunosuppressed (e.g. organ transplant recipients).
Microscopic
Features:[19]
- Nests or sheets or trabeculae.
- Scant cytoplasm.
- Nuclear moulding.
- Multiple small nucleoli.
- Usually mitotically active.
Image:
IHC
- CK7 -ve, CK20 +ve
Eccrine carcinoma
General
- Arises from the proximal sweat duct.
Microscopic
Features:
- Pleomorphic nuclei with nucleoli.
- Duct-like structures - key feature.
- Extends from dermis into epidermis (follows path of a benign sweat duct).
Image: Eccrine carcinoma - intermed. mag. (WC).
Eccrine poroma
General
- Benign tumour arising from the distal sweat duct.
- Erythematous - gross.
Microscopic
Features:[20]
- Broad sheets of basaloid cells containing ductal structures - key feature.
- Biphasic stroma:
- Edematous stroma.
- Sclerotic stroma.
- Moderate nuclear pleomorphism.
- +/-Occasional mitoses.
Notes:
- Area above gland appears crusted.
Kaposi sarcoma
- See Kaposi sarcoma.
See also
References
- ↑ 1.0 1.1 Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1180. ISBN 978-1416031215.
- ↑ RS. 17 May 2010.
- ↑ URL: http://emedicine.medscape.com/article/1101146-diagnosis. Accessed on: 6 May 2010.
- ↑ 4.0 4.1 Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1180-1. ISBN 978-1416031215.
- ↑ URL: http://education.vetmed.vt.edu/curriculum/VM8054/labs/Lab2/Examples/exfontana.htm. Accessed on: 5 May 2010.
- ↑ Ramos-Herberth FI, Karamchandani J, Kim J, Dadras SS (September 2010). "SOX10 immunostaining distinguishes desmoplastic melanoma from excision scar". J. Cutan. Pathol. 37 (9): 944–52. doi:10.1111/j.1600-0560.2010.01568.x. PMID 20653825.
- ↑ 7.0 7.1 Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1183. ISBN 978-1416031215.
- ↑ AP. May 2009.
- ↑ 9.0 9.1 Abenoza P, Lillemoe T (October 1993). "CD34 and factor XIIIa in the differential diagnosis of dermatofibroma and dermatofibrosarcoma protuberans". Am J Dermatopathol 15 (5): 429–34. PMID 7694515.
- ↑ 10.0 10.1 Goldblum JR, Tuthill RJ (April 1997). "CD34 and factor-XIIIa immunoreactivity in dermatofibrosarcoma protuberans and dermatofibroma". Am J Dermatopathol 19 (2): 147–53. PMID 9129699.
- ↑ URL: http://emedicine.medscape.com/article/1099540-overview. Accessed on: 24 August 2010.
- ↑ URL: http://emedicine.medscape.com/article/1099540-overview. Accessed on: 24 August 2010.
- ↑ URL: http://emedicine.medscape.com/article/1098342-overview. Accessed on: 24 August 2010.
- ↑ 14.0 14.1 Klatt, Edward C. (2006). Robbins and Cotran Atlas of Pathology (1st ed.). Saunders. pp. 385. ISBN 978-1416002741.
- ↑ URL: http://www.mdconsult.com/das/book/body/199872830-2/0/1709/I4-u1.0-B978-0-443-06694-8..50117-2--f2.fig. Accessed on: 6 May 2010.
- ↑ Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1185. ISBN 978-1416031215.
- ↑ 17.0 17.1 Calder, KB.; Smoller, BR. (May 2010). "New insights into merkel cell carcinoma.". Adv Anat Pathol 17 (3): 155-61. doi:10.1097/PAP.0b013e3181d97836. PMID 20418670.
- ↑ Pulitzer, MP.; Amin, BD.; Busam, KJ. (May 2009). "Merkel cell carcinoma: review.". Adv Anat Pathol 16 (3): 135-44. doi:10.1097/PAP.0b013e3181a12f5a. PMID 19395876.
- ↑ Humphrey, Peter A; Dehner, Louis P; Pfeifer, John D (2008). The Washington Manual of Surgical Pathology (1st ed.). Lippincott Williams & Wilkins. pp. 491. ISBN 978-0781765275.
- ↑ URL: http://www.pathconsultddx.com/pathCon/diagnosis?pii=S1559-8675(06)70190-5. Accessed on: 2 July 2010.