A Manual of Clinical DiagnosisTodd, James Campbell
Science
A Manual of Clinical Diagnosis
Todd, James Campbell
Diagnosis, Laboratory
(3) Splenic Anemia.--This is an obscure form of anemia associated with
great enlargement of the spleen. It is probably a distinct entity.
There is decided decrease of hemoglobin and red corpuscles, with
moderate leukopenia and relative lymphocytosis. Osler's fifteen cases
averaged 47 per cent. hemoglobin and 3,336,357 red cells. Stained
films show notable irregularities in size, shape, and staining
properties only in advanced cases. Erythroblasts are uncommon.
B. LEUKEMIA
Except in rare instances, diagnosis is easily made from the blood
alone. Two types of the disease are commonly distinguished: the
_myelogenous_ and the _lymphatic_. Atypical and intermediate forms are
not uncommon. Pseudoleukemia, because of its clinical similarity to
lymphatic leukemia, is generally described along with leukemia.
1. Myelogenous Leukemia.--This is usually a chronic disease, although
acute cases have been described.
Hemoglobin and red corpuscles show decided decrease. The color-index
is moderately low.
Most striking is the immense increase in number of leukocytes. The
count in ordinary cases varies between 100,000 and 300,000. Counts
over 1,000,000 have been {209} met. During remissions, the leukocyte
count may fall to normal.
While these enormous leukocyte counts are equaled in no other disease,
and approached only in lymphatic leukemia and extremely high-grade
leukocytosis, the diagnosis, particularly during remissions, depends
more upon qualitative than quantitative changes. Although all
varieties are increased, the characteristic and conspicuous cell is
the myelocyte. This cell never appears in normal blood; extremely
rarely in leukocytosis; and never abundantly in lymphatic leukemia. In
myelogenous leukemia myelocytes usually constitute more than 20 per
cent. of all leukocytes. Da Costa's lowest case gave 7 per cent. The
neutrophilic form is generally much more abundant than the
eosinophilic. Both show considerable variations in size. Very constant
also is a marked absolute, and often a relative, increase of
eosinophiles and basophiles. Polymorphonuclear neutrophiles and
lymphocytes are relatively decreased.
[Illustration: FIG. 85.--Blood from a case of splenomedullary
leukemia, stained with Ehrlich's triple stain (Jakob).]
{210} The red cells show the changes characteristic of a severe
secondary anemia, except that nucleated reds are commonly abundant; in
fact, no other disease gives so many. They are chiefly of the
normoblastic type. Megaloblasts are uncommon. Blood-plaques are
generally increased.
[Illustration: FIG. 86.--Blood: Lymphatic leukemia (lower section);
marked leukocytosis (upper section). Stained smears. Compare types of
leukocytes with Fig. 85 (from Greene's "Medical Diagnosis").]
2. Lymphatic Leukemia.--This form may be either acute or chronic.
There is marked loss of hemoglobin and red corpuscles. The color-index
is usually moderately low.
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