2. OVERVIEW
⢠Introduction
⢠Head to Toe Examination
-Site specific markers
-Site non-specific markers
⢠Classifying Markers & Associated Malignancies
3. INTRODUCTION
⢠Skin - a mirror for underlying malignancies.
⢠Skin manifestation - may be the only symptom
of underlying malignancy.
⢠A keen eye is, therefore, required to diagnose
them.
5. (a) Both conditions start at the same time,
(b) both conditions follow a parallel course,
(c) the condition is not recognized as a part of a
genetic syndrome,
(d) a specific tumor occurs with a certain
dermatosis,
(e) Genetic association is present, and
(f) a high percentage of the statistical association is
noted.
CURTHâS POSTULATES
50. DIRECT EXTENSION
1. Tumor spillage - FNAC, pleural biopsy, draining
malignant ascites, lap, sx
2. Carcinoma erysipeloides - Tumor cells in lymphatics;
erysipelas-like picture; CA breast.
3. Carcinoma en cuirasse â sclerotic infiltration of CA
breast
4. Carcinoma telangiectodes â telengiectatic
infiltration of CA breast
5. Pagetâs disease â extension from underlying ductal
tumor of breast
60. DISEASE FEATURES MALIGNANCY
Gardnerâs syndrome multiple epidermoid
cysts, fibromas, and
pilomatrixomas
GI malignancy
PeutzâJeghers
syndrome
mucocutaneous
pigmentation in peri-
and intra-oral
regions
GI malignancy
HowelâEvans
syndrome
PPK Oesophageal CA
Gorlin syndrome multiple basal cell
carcinomas,
mandibular
keratocysts,
dyskeratotic pits of
palms, and soles
medulloblastoma
and ovarian tumors
61. DISEASE FEATURES MALIGNANCY
Dysplastic nevus
syndrome
multiple atypical
melanocytic nevi
pancreatic,
gastrointestinal,
lung, breast, and
laryngeal carcinoma
Xeroderma
pigmentosum
Photosensitivity,
myriads of lentigines
ocular, and
cutaneous
malignancy
Von Hippel-Landau
syndrome
hemangiomas and
cafe-au-lait spots
hemangioblastoma
of CNS,
pheochromocytoma,
renal and pancreatic
cancers
Neurofibromatosis
type 1 and 2
multiple peripheral
neurofibromas, cafe-
au-lait macules,
axillary freckles
CNS tumors
62. DISEASE FEATURES MALIGNANCY
Carneyâs syndrome lentigines, atrial
myxomas,
mucocutaneous
myxomas, blue nevi
gonadal hormone
secreting tumors,
malignant thyroid
tumors
Cowdenâs disease warty âcobblestoneâ
hyperplasia of the
mucosal surfaces,
acral warty keratosis,
and punctuate
keratosis
GI polyposis and cysts
and breast
adenocarcinoma
MuirâTorre syndrome sebaceous lesions
and keratoacanthoma
HNPCC
Bloom syndrome sun sensitive
telangiectasia, cafe-
au-lait macules
lymphoproliferative
neoplasia
70. BULLOUS DISORDERS
⢠Paraneoplastic pemphigus - NHL, Castleman tumor,
thymoma
⢠Pemphigus - Thymoma, Hodgkinâs disease.
⢠Herpes gestationis - hydatidiform mole and germ
cell tumor.
⢠EBA - CA of bronchus and multiple myeloma
⢠LAD - Lymphoma, CLL, carcinoma bladder and
esophagus, and hydatidiform mole
⢠Cicatricial pemphigoid - CA lung, stomach, colon,
and endometrium
71. KERATINIZATION DISORDERS
⢠Acanthosis nigricans - Gastric and intra-abdominal
adenocarcinoma.
⢠Acquired ichthyosis - Hodgkinâs lymphoma,
carcinoma lung, breast, and cervix.
⢠Palmer hyperkeratosis - Esophageal carcinoma.
⢠Palmoplantar keratoderma - Breast or ovarian
carcinoma.
⢠Tripe palms - Gastric and lung carcinoma.
⢠Erythroderma - Leukemia, lymphoma, MF.
72. ⢠Bazex - SCC of oropharynx, larynx, lung, esophagus,
and thymus.
⢠Florid cutaneous papillomatosis - CA stomach,
breast, lungs, and ovary.
⢠Sign of LeserâTrelat - Adenocarcinoma of stomach
or colon.
⢠Multiple cherry angiomas are associated with solid
tumors.
⢠Multiple skin tags are associated with colonic
polyps.
⢠P. Rotunda â HCC
73. COLLAGEN VASCULAR DISORDERS
⢠Dermatomyositis - CA ovary, lung, pancreas,
stomach, colorectal, and lymphoma.
⢠Lupus erythematosus - Lymphoma, thymoma.
⢠Scleroderma - CA lung, esophagus.
⢠Systemic lupus erythematosus - Lymphoreticular
malignancies, myeloma, and paraproteinemias.
Bazex - symmetric erythematous and violaceous scaly papules on hands, feet, knees, ears, and nose
Extra mammary pagetâs â erythematous plaques in perianal and scrotal skin
dysplastic nevus syndrome
Sebaceous adenoma â erythematous nodule with central umbilication
POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes)
arise from the arrectores pilorum muscles and occur as grouped, linear, or segmentally distributed firm, red to brown intradermal papules and nodules, which are fixed to the skin, but free from the deeper tissues
DKC = Reticulate hyperpigmentation, nail dystrophy, leucoplakia, bonemarrow failure and increased risk of malignancy (e.g. mucosal squamous cell carcinoma, leukaemia, Hodgkin
disease) are the hallmarks.
fixed, annular, scaly, noninflamed, and hyperpigmented lesions
EGR â Wood-grain appearance
NME - erythema, vesicles, pustules, bullae and erosions involving face, intertriginous area, and perigenital region
EGR - erythematous bands moving in waves over the body
NME - erythema, vesicles, pustules, bullae and erosions involving face, intertriginous area, and perigenital region
EGR - erythematous bands moving in waves over the body