Splenomedullary Leucemia

(MYELOID LEUCEMIA; MYELEMIA)

Myelemia is a disease characterized by an enormous increase in the

white cell content with proportionate changes in the spleen, liver, and

the blood marrow.

=Etiology.=—It is a disease occurring at all ages, but the majority of

cases are recognized in adult males.

Heredity, trauma to the spleen, malaria, syphilis, and rapid repetition

of pregnancies seem to be at least exciting factors. A few cases have

been reported in which tenth, eleventh, and twelfth rib lesions were

definite etiologic factors by pressure.

=Diagnosis.=—The patient goes through a period of vague, indefinite,

and wandering symptoms. General malaise, weakness often accompanied by

dyspnea, and emaciation similar in many ways to incipient pulmonary

tuberculosis, except that the slight temperature changes are not

typical. At the same time there may be digestive discomfort of

various kinds without typical pathology. Of these early symptoms the

most persistent is the =dyspnea= which is a structural result of the

increase in size of the spleen. As a direct pressure result of this

hyperplasia, there may develop dropsical infiltration of the lower

extremities and ascitic accumulation in the abdominal cavity.

With the changes in the blood itself, the blood vessel walls break down

more easily, and subcutaneous hemorrhages, epistaxis and hematemesis

are common.

In an attempt to destroy the excessive amount of white cells, the liver

may become enlarged. But this occurs later and of much less degree

than the enormous increase in size of spleen. There may be areas of

hemorrhage with resulting softening in the spinal cord. The most likely

areas to suffer are the posterior and lateral horns, with resulting

paraplegia, spastic or ataxic.

Usually, the course is slow, and the condition is truly chronic. But,

occasionally, the rapid increase and succession of symptoms, with

concomitant blood changes, change the diagnosis to acute myelogenous

leukemia.

The total cell count, red plus white, is diminished, for while there is

enormous relative increase of the white cells a greater actual decrease

takes place in the reds. This decrease in reds is partially relative

from crowding out of erythrocytes by leucocytes, but there is also

actual decrease in their formation, so that there is an actual anemia

present as well as a leukemia.

In some respects the red cells behave as in chlorosis, each carrying

a diminished percentage of hemoglobin, resulting in a low color

index. Atypical staining reactions and morphology, together with many

fractured forms, are the rule. Normoblasts are common throughout the

course of the disease, but megaloblasts seldom appear until near fatal

termination.

The changes in the white cells are enormous, both as to numbers and

character of cells found. The total white count often exceeds 350,000.

This, with the accompanying reduction in number of erythrocytes,

leads to a reduction of the ratio between reds and whites to as low

as 1 to 5 or 3, or occasionally 1 to 1. There is an actual increase

in number of all the white cells with the possible exception of the

lymphocytes. In the actual increase of polymorphonuclear neutrophiles

and eosinophiles is rendered a sharp relative decrease by the enormous

production of myelocytes. Basophiles are usually both relatively and

absolutely increased. In a white count of 350,000 it is not unusual to

have present 325,000 myelocytes, with 25,000 as the actual number of

ordinary leucocytes. There is, therefore, a =mild leucocytosis= coupled

with a =violent= leukemia. These two are combined with an =anemia= that

varies with the course of the disease.

=Treatment.=—The treatment is largely hygienic, including thorough

osteopathic attention to the lower dorsal and costal area. Symptomatic

treatment is often followed by temporary improvement both clinically

and in the blood picture, but complete recovery seldom takes place.

Occasionally, roentgen therapy has given a “cure” lasting several years.

=Prognosis= is not good. These patients are frequently carried away

quickly by some oftentimes slight intercurrent infection. Even if

carefully guarded from such, the course of the process usually leads to

death from exhaustion in two or three years.

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