Cases of general idiopathic atrophy of the skin have from time to {684}

time been reported, the disease in almost all instances being more

marked in some localities than in others, occurring in the form of more

or less extensive patches. The disease originally described by Hebra

and Kaposi with the name xeroderma, or parchment-skin disease, may here

be referred to. The lesions consist of numerous disseminated

pigment-spots, resembling freckles; telangiectases, or minute congeries

of blood-vessels; atrophic macules of variable size; with more or less

shrinking and contraction of skin, followed in most cases by

epitheliomatous tumors and ulceration. The disease almost invariably

begins in early years, is prone to show itself in several children of

the same family, and lasts during life. The advanced stages of

scleroderma and morphoea likewise show marked atrophic changes, which,

however, will be considered in speaking of those diseases.

Senile Atrophy.--This form of atrophy, taking place as the result of

old age, may be simple or degenerative, both usually occurring

together. The integument becomes thin and wasted, the surface being

dry, wrinkled and more or less discolored by pigmentation, with loss of

hair. In degenerative atrophy the connective tissue of the corium

becomes changed into a fine or coarse granular matter or into a

homogeneous vitreous mass. Fatty metamorphosis and marked pigmentary

deposits are also common.

Maculæ et Striæ Atrophicæ.--Atrophic streaks and spots may occur

idiopathically or symptomatically. The idiopathic form is that most

frequently encountered, and occurs without known cause, generally

making its appearance insidiously. It is characterized by lines or

streaks constituting the so-called linear atrophy, striæ atrophicæ; or

by spots, maculæ atrophicæ. The streaks are more frequently met with,

and consist of irregular curved or tortuous lesions, usually about a

line in width and of variable length, running parallel with one

another. The macules are rounded or ovalish, varying in size from a

pinhead to a finger-nail. Both are smooth and glistening, and the skin

is thinned and scar-like. They are slightly depressed or grooved, and

possess a pinkish, whitish, or bluish-gray color. They may appear upon

any region, but the abdomen, buttocks, and thighs are the favorite

localities. They pursue a slow course over a period of years or a

lifetime, occasioning no inconvenience. The first stage of either

variety of the disease is characterized by erythema, the lesion being

reddish, hyperæmic, and slightly raised or puffed. This sooner or later

disappears, followed by depression and atrophy.

The symptomatic form of the affection is usually noted to take place as

the result of extreme distension of the cutaneous structures. It occurs

sometimes in obese subjects, and in the latter stages of pregnancy upon

the abdomen and mammæ, and over large abdominal and other tumors where

the skin is greatly stretched, constituting the so-called lineæ

albicantes.

{685} CLASS VI.--NEW GROWTHS.[6]

[Footnote 6: Lepra (leprosy), an important disease of this class,

appears, in Vol. I. p. 785, as a separate article by J. C. White.]

Keloid.

Keloid is a connective-tissue new growth, characterized by one or more

irregularly-shaped, variously-sized, elevated, smooth, firm, somewhat

elastic, pale-reddish, cicatriform lesions. It ordinarily begins as a

nodule or tubercle, pea- or bean-sized, which slowly, usually in the

course of years, increases in dimension. When fully developed, the

growth appears as an ovalish, elongated, cylindrical, fungoid or

crab-shaped patch, occupying usually an area of one or several inches,

distinctly elevated, sharply defined, and firmly implanted in the skin.

In some cases the lesion does not exceed the size of a pea or a bean.

The color is usually pinkish-white. The surface is smooth, shining, and

commonly devoid of hair, with no tendency to scaliness or ulceration,

and generally marked by ramifying vessels. It is firm and elastic to

the touch. The disease sometimes appears in the form of streaks or

lines. It is seen most frequently upon the sternum, although other

regions, as the neck, mamma, ear, sides of the trunk, or back are often

invaded. It is more common in the colored race. The lesion is usually

single, though several may coexist. Itching to a slight degree is

sometimes present, and more or less pain, especially on pressure, may

also exist. Depending upon the origin of the growth, whether arising

spontaneously or upon the site of various injuries of the skin, keloid

is termed, respectively, spontaneous, or true, and cicatricial, or

false. Clinically and pathologically, both varieties are the same.

It is often met with as the result of burns, cuts, flogging, and all

ulcerative affections. Not infrequently it takes its origin in the

scars of acne and variola; occasionally it is seen to develop on the

lobe of the ear, taking its start at the point where the ear has been

pierced. Pathologically, the lesion is a connective-tissue new growth,

made up of a dense, fibrous mass of tissue, whitish in color, having

its seat in the corium. The clinical features of keloid are so

characteristic that no difficulty is experienced in recognizing it. The

course of the disease is chronic, usually lasting throughout life; in

exceptional instances spontaneous involution has been noted.

Treatment is usually negative. Removal by excision or caustics is, as a

rule, followed by a return of the growth, and sometimes in an

aggravated form. If its destruction or extirpation is decided upon, it

should not be done while the growth is still progressive. Improvement

has been reported by Vidal from multiple linear scarification. If the

formation is painful, various anodyne applications may be made. Iodine,

mercurial, and lead plasters may be tried with the object of promoting

absorption. Painting the growth with a solution composed of potassium

iodide one drachm, and an ounce each of soft soap and alcohol, followed

by the application of lead plaster spread on a piece of soft leather,

has been advised by Wilson. The use of lead plaster alone, applied

continuously as a plaster, is sometimes followed by softening and

diminution in size.

{686} Fibroma.

Fibroma (molluscum fibrosum, fibroma molluscum) is a connective-tissue

new growth, characterized by sessile or pedunculated, soft or firm,

rounded, painless tumors, varying in size from a pea to an egg or

larger, seated beneath and in the skin. A single growth may occur, or,

as is more commonly the case, they are present in large numbers, and

usually scattered over the greater portion of the body, having a

preference for the softer tissues,--for example, the trunk. They may be

of various shapes, rounded and sunken in the skin itself or in the

subcutaneous tissue, or club- or pear-shaped and pedunculated. They

usually begin as soft masses in the skin. If but one tumor exists, it

is apt to be pedunculated or pendulous, and to attain considerable

dimensions, in some cases weighing several pounds. In these instances

surface-ulceration is occasionally noted as the result of mere weight

or pressure. As commonly met with, however, the growths are numerous,

several hundreds existing, varying from a pea to a cherry in size, with

larger ones scattered here and there. The overlying skin is normal,

pinkish or reddish, or may be loose or stretched, hypertrophied or

atrophied. They are unattended with pain. They may make their

appearance at any age, often in childhood, and grow as a rule slowly.

After reaching a certain size they are apt to remain stationary; in

rare instance spontaneous involution of some of the growths has been

noted to take place. The affection is not common. It is often

inherited, and may show itself in several members of the same family.

Those in whom it is observed are usually noted to be stunted in their

physical and mental development. The general health is not involved.

Opinions are divided as to whether the growths take their origin in the

connective-tissue framework of the fatty tissue, in the connective

tissue of the corium, or in that of the walls of the hair-sac. The

developed tumors consist of a connective-tissue capsule enclosing a

whitish fibrous mass, with the central portion more or less soft and

pulpy, out of which may be squeezed a small quantity of yellowish

fluid. Small, recent tumors are composed of gelatinous, newly-formed

connective tissue, while old growths consist entirely of a dense,

firmly-packed fibrous tissue.

They are to be distinguished from the tumors of molluscum epitheliale

by the absence of an aperture or depression upon their summits. They

can scarcely be confounded with multiple neuromata or with lipomata, as

the accompanying pain of the former and the lobulated structure and

soft feel of the latter are sufficiently distinctive. Their removal, if

desired, may be effected by the knife, or in the case of the large and

pedunculated growth by the ligature or by the galvano-cautery.

Neuroma.

Neuroma cutis, or neuroma of the skin, is characterized by the

formation of variously-sized fibrous tubercles, containing new

nerve-elements, having their seat primarily in the corium, and

accompanied in their development by violent paroxysmal pain. It is

exceedingly rare, there being but few cases recorded. It appears on the

shoulders, arms, thighs or buttocks in the form of numerous,

disseminated, pinhead to hazelnut in {687} size, round or ovalish

tubercles or nodules, which at the outset may be either painful or

painless; in the later stages, however, pain, both spontaneous and upon

pressure, is a constant symptom. The growths are firm, immovable, and

elastic, and are seated in the corium, extending into the deeper

structures. They may be covered scantily with fine, laminated,

glistening scales, as in the case reported by one of us. Anatomically,

the tumors are composed of nerve-fibres, yellow elastic tissue,

blood-vessels, and lymphoid cells. Excision of a portion of the

nerve-trunk leading to the affected area has been practised in one case

(Kosinski's) reported, with permanent relief; in another (Duhring's)

the relief was merely temporary.

Xanthoma.

Xanthoma (also called vitiligoidea and xanthelasma) is a

connective-tissue new growth, characterized by the formation of

yellowish, circumscribed, irregularly-shaped, variously-sized,

non-indurated, flat or raised patches or tubercles. Two varieties are

met with. The macular, or flat form (xanthoma planum) is commonly seen

upon the eyelids, looking not unlike pieces of chamois-skin inserted in

the lids. This form may also be encountered occasionally on other parts

of the face, as well as upon the body. The patches are smooth, opaque,

usually sharply defined, and to the touch soft and apparently normal in

texture; they are on a level with the surrounding integument or

slightly raised, and of a creamy or yellowish color. They vary in size

and shape, and may coalesce, forming a band extending across the

eyelids, especially the upper lids. The tubercular form (xanthoma

tuberosum) is usually met with upon the neck, trunk, and extremities,

the eyelids seldom being invaded. It occurs as small, isolated nodules,

or in patches slightly raised above the level of the skin, consisting

of aggregations of tubercles of the size of a milletseed or larger.

Both forms of the disease not infrequently occur in the same

individual. After reaching a certain development it is apt to remain

stationary throughout life, and with no involvement of the general

health. As a rule, the lesions are few in numbers; on the other hand,

rarely they may be numerous (xanthoma multiplex). The affection is

usually encountered in middle and advanced life, although it is

occasionally met with in the young. It is more common in women than in

men. Jaundice has been frequently noticed as preceding or accompanying

it, especially the tubercular variety. Pathologically, it is a

connective-tissue new growth with fatty degeneration. Excision, where

practicable, constitutes the sole method of treatment.

Myoma.

Myoma cutis, or dermato-myoma (known also as liomyoma cutis), is a rare

affection, consisting of tumors of the skin composed of muscular

fibres. They occur either as single or multiple tumors, varying in size

from a lentil to an egg, localized in a special region, as the nipple,

scrotum, labia majora, thigh, hand, or foot; or, more rarely, numerous,

and scattered over the greater portion of the whole body. They are

{688} either flat or pedunculated, rounded or oval in form, pale-red in

color, with a smooth surface; although generally painless, they are

sometimes tender upon pressure, The growth consists essentially of a

new formation of unstriped muscular fibres. At times it is composed

largely of connective tissue (fibromyoma), or it may contain an

abundance of blood-vessels, giving rise to cavernous erectile tumors

(myoma telangiectodes). The disease is benign.

Angioma.

Angioma, or nævus vasculosus, is a congenital formation composed

chiefly of blood-vessels and having its seat in the skin and

subcutaneous tissue. Several forms of the affection are met with, all

of which, however, may be grouped under two heads--non-elevated and

prominent. The former (nævus flammeus, nævus simplex, angioma simplex)

is illustrated by the so-called port-wine mark, or claret-stain, known

in German as feuermal, and in French as tache de feu. The prominent

variety (angioma cavernosum, nævus tuberosus) may be turgescent,

erectile, pulsating, tumor-like, circumscribed growths, with an uneven

or rugous surface. In shape nævi are usually roundish, but may be

irregular; in color, bright or dark red, violaceous, or bluish; and in

size as large as a pea or a bean, or in some cases involving areas

several inches in diameter. As a rule, they are single formations. They

may occur on any part of the body, but are most frequently seen about

the face. Their course varies. In many instances, after attaining a

certain size, they remain stationary, or in some cases may retrograde

or undergo spontaneous involution, this remark applying more

particularly to the flat variety in early life. Ordinarily, they are

permanent deformities. They become pale under pressure, and the more

prominent growths are markedly compressible. Anatomically, the growth

consists of a dilatation and hypertrophy of the arterial and venous

blood-vessels of the corium and subcutaneous tissues, and in some

instances there is increase in connective tissue. In some cases the

connective-tissue hypertrophy is made up mainly from the adipose layer

(angioma lipomatodes). Occasionally there may be more or less

pigmentation.

In the treatment, the extent, form, and region involved are to be

considered. Various methods have been advised for their removal. For

pinhead-sized nævi puncturing with a red-hot needle, or with a needle

charged with nitric or chromic acid, may be employed. Those of pea size

may be treated by caustic applications. Sodium ethylate, as recommended

by Richardson, is an efficient caustic for the more superficial forms:

it should be pure and applied with a glass rod; a dry dressing is to be

employed and the crust permitted to loosen itself. Painting a nævus

with liquor plumbi subacetatis will, if repeated daily for several

weeks or months, sometimes succeed. Caustic potash in solution, from

one to two drachms in the ounce, and nitric acid, may both be

cautiously used. An ointment of a drachm of adhesive plaster and nine

grains of tartar emetic applied to small nævi will, according to

Neumann, cause free suppuration and healing. A solution of eight grains

of corrosive sublimate in a drachm of collodion is sometimes effective.

Injections of astringent and irritating liquids, such as the tincture

of the chloride {689} of iron and cantharidine, as formerly practised,

possess no advantage over safer methods. Linear and punctate

scarifications--in the latter the needles being charged with a 50 per

cent. solution of carbolic acid or a 25 per cent. solution of chromic

acid--have been recommended. In small formations vaccinating the nævus

is often successful. The galvano-cautery and the actual cautery are

both serviceable in treating the smaller nævi. Electrolysis constitutes

a valuable plan of treatment. A current of from six to twelve cells is

usually required. One or more platinum needles are attached to the

negative pole and a single needle or charcoal point to the positive

pole. Slight frothing at the points of insertion indicates that the

action has been sufficient. Suppuration and sloughing should not occur

if proper care is exercised. If the nævus is extensive, only a small

portion is to be treated at the one sitting. In the port-wine mark this

method promises the best results; the color is made much lighter, and

exceptionally is made to disappear entirely. In prominent, and

especially in pedunculated, tumors a ligature may be employed.

Lymphangioma.

Lymphangioma (also described as lymphangioma tuberosum multiplex) is a

rare disease, characterized by numerous, scattered, pea- or bean-sized,

ovalish or rounded, brownish-red, glistening, smooth, slightly-elevated

tubercles, having a somewhat translucent look, occurring for the most

part about the trunk. They are firm and elastic to the touch; are

situated in the cutis, but are not sharply defined; they can be readily

made to sink below the level of the surrounding integument, owing to

their marked compressibility. At times they have a lilac or bluish

tinge. The growths bear some resemblance to the large papular

syphiloderm. They are generally congenital or appear in childhood.

Anatomically, they consist of immensely dilated and hypertrophied

lymphatic vessels. The course of the disease is slow, and evinces no

disposition to malignancy. The general health is not involved.

Lupus Erythematosus.

Lupus erythematosus (also known as lupus erythematodes, seborrhoea

congestiva, and lupus sebaceus) is a small-celled new growth,

characterized by one or more circumscribed, variously sized and shaped,

reddish patches, more or less covered with adherent grayish or

yellowish scales. The affection usually begins as a rounded,

circumscribed, pinhead- to pea-sized, slightly elevated lesion, which

increases in size by peripheral extension until considerable surface is

involved; or, as is often the case, the disease starts with several

such spots, which grow and generally coalesce, sooner or later

involving considerable surface. The spots are at first erythematous and

slightly scaly, with but little elevation, later becoming thickened,

with a more or less raised border sharply defined against the healthy

skin, covered with small, firmly adherent yellowish or grayish scales,

with enlarged and plugged or patulous follicles, the centre of the

patch being somewhat depressed. The color is pinkish, reddish, or {690}

violaceous. In the beginning the disease often closely resembles

seborrhoea,--so much so that it was originally described by Hebra as

seborrhoea congestiva. The scaling is usually scanty, but in

exceptional instances may be abundant. At times the lesions show little

tendency to peripheral growth, the large areas of disease resulting

from the continuous appearance of new patches in proximity which run

together. Occasionally the patches are small, discrete, and numerous,

when the disease is apt to be disseminated over considerable surface.

Lupus erythematosus is seen most frequently about the face, one or

several patches, varying in size from a pea to a silver dollar,

ordinarily being present. The nose and the cheeks are favorite

localities, and, seated here, the disease is apt to be symmetrical,

extending from one cheek across the nose to the other cheek, in shape

representing rudely the outline of a bat or butterfly with outstretched

wings. The lips, ears, scalp, and other parts of the body are often

affected. The progress of the disease is variable; the patches, as a

rule, reach a certain size, and then remain stationary or retrogress,

or, as generally happens, the central portion becomes depressed and

more or less atrophied. The resulting scar is whitish, usually soft,

punctate, and superficial. As old patches disappear it is not uncommon

to see new patches appearing close by. It is essentially a chronic

disease: the individual lesions may be acute in their course, and when

such is noted, as a rule new areas of disease continue to appear in

rapid succession. Ordinarily, however, the individual patches

themselves are chronic in their course. The disease is not attended

with ulceration. The subjective symptoms of itching and burning are

usually mild in character, and sometimes are entirely wanting.

The condition of the general health is, as a rule, good. The disease is

seen more frequently in women than in men, and is rarely observed

before puberty, being chiefly encountered in early adult and middle

age. The causes are not known. It frequently begins as a seborrhoea,

but it may occur (although rarely) upon the palms of the hands, where

sebaceous glands are not to be found. It is a notable fact, however,

that the disease is most commonly encountered in those who are subject

to disorder of these glands. It is observed more often in persons of

light complexion. It is comparatively rare. The condition of the

general health apparently exercises no causative influence.

Pathologically, the process is essentially a chronic inflammation of

the cutis, superinducing degenerative and atrophic changes. In the

majority of cases the disease originates in the sebaceous glands, but

later all parts of the skin become affected. It is even authoritatively

stated that it may in some instances take its start in the subcutaneous

connective tissue. In some respects it has the character of a new

growth, which until late years it has been considered. In the light of

recent investigations, however, it seems possible that it may be a

chronic inflammation leading to degenerative changes. The process never

ends in the formation of pus. There is small-celled infiltration about

the follicles and glands, the blood-vessels are dilated, the

surrounding tissue is infiltrated with embryonic corpuscles, and the

sebaceous glands are enlarged and their walls infiltrated with small

cells. The whole affected area is, in fact, infiltrated with a

small-celled inflammatory new growth. If retrograde changes occur, the

{691} infiltration may disappear by absorption without leaving a trace.

On the other hand, and as is usually the case, degenerative

metamorphosis, resulting in absorption and atrophy, takes place.

A system of practical medicine. By American authors. Vol. 4 · 第 90 / 116 段