Professional Documents
Culture Documents
Shaoshan Tang, MD,1 Tadashi Shimizu, MD,1 Yoichi Kikuchi, MD,1 Sumiyo Shinya, MD,1
Riwa Kishimoto, MD,1 Yasunori Fujioka, MD,2 Kazuo Miyasaka, MD1
1
Department of Radiology, Hokkaido University School of Medicine, North-5, West-7, Kita-ku,
Sapporo 060-8638, Japan
2
Department of Pathology, Kyorin University School of Medicine, Shinkawa 6-20-2, Mitaka,
Tokyo 181-8611, Japan
DISCUSSION
Splenic hamartoma, variously termed splenoma,
spleno-adenoma, fibrosplenoma, and nodular hy-
perplasia of the spleen, is a rare, benign tumor
with an autopsy incidence of 0.13%.1 Since the
first description by Rokitansky in 1861,6 more
than 100 cases have been reported. In none of
these cases was a definite diagnosis made preop-
eratively.
Two histologic types of splenic hamartoma
have been described: the white-pulp (lymphoid)
type and the red-pulp (pulposal) type. The white-
pulp type is composed entirely of lymphoid tissue.
The red-pulp type, defined by the Armed Forces
FIGURE 1. Gray-scale sonogram shows a grossly homogeneous, hy- Institute of Pathology as a hamartoma in 1995,7
poechoic mass (arrows) at the lower pole of the spleen.
is composed of sinuses and structures histologi-
cally similar to that of normal splenic red pulp.1
A splenic hamartoma shows expansive growth
A splenectomy was performed because a malig- and compresses the surrounding splenic tissue
nant splenic neoplasm or metastasis could not be without a true capsule. The hamartomas were
ruled out. On gross examination, there were mul- red-pulp type in most of the reported cases and in
tiple solid nodules in the spleen ranging from 0.5 all of the reported cases in which the hamartomas
cm to 2 cm and slightly grayer in color than the were symptomatic.1,2 It is sometimes difficult to
surrounding splenic parenchyma. Histologic ex- delineate the red-pulp type hamartoma from nor-
amination of the lesions showed dilated vessels mal splenic tissue because this hamartoma con-
and congestion. The masses were composed of red sists of abnormal mixtures of normal splenic ele-
pulp; they lacked fibrous trabeculae and white ments. Fine-needle aspiration biopsy is not
pulp (Figure 6). The normal splenic parenchyma recommended as a diagnostic tool because there is
FIGURE 2. Color Doppler sonogram shows multiple vessels within the mass (arrows).
FIGURE 3. Duplex Doppler sonogram shows arterial flow in the mass (arrows). The peak systolic velocity was
71.4 cm/second, with a resistance index of 0.525 and a pulsatility index of 0.776.
puted tomography and ultrasonic findings. Clin appearances of splenic hamartoma. J Comput As-
Radiol 1992;45:410. sist Tomogr 1992;16:425.
6. Morgenstern L, McCafferty L, Rosenberg J, et al. 12. Kishikawa T, Numaguchi Y, Watanabe K, et al.
Hamartomas of the spleen. Arch Surg 1984;119: Angiographic diagnosis of benign and malignant
1291. splenic tumors. AJR Am J Roentgenol 1978;130:
7. Warnke RA, Weiss LM, Chan JK, et al. Tumors of 339.
the lymph nodes and spleen. In: Rosai J, Sobin LH, 13. Niizawa M, Ishida H, Morikawa P, et al. Color
editors. Atlas of tumor pathology. Series 3, Fascicle Doppler sonography in a case of splenic hemangi-
14. Washington, DC: Armed Forces Institute of Pa- oma: value of compressing the tumor. AJR Am J
thology; 1995. Roentgenol 1991;157:965.
8. Kumar PV. Splenic hamartoma. A diagnostic prob-
14. Ito K, Mitchell DG, Honjo K, et al. MR imaging of
lem on fine needle aspiration cytology. Acta Cytol
acquired abnormalities of the spleen. AJR Am J
1995;39:391.
Roentgenol 1997;168:697.
9. Wirbel RJ, Uhlig U, Futterer KM. Case report:
splenic hamartoma with hematologic disorders. 15. Ha HK, Kim HH, Kim BK, et al. Primary angio-
Am J Med Sci 1996;311:243. sarcoma of the spleen. CT and MR imaging. Acta
10. Ferguson ER, Sardi A, Beckman EN. Spontaneous Radiol 1994;35:455.
rupture of splenic hamartoma. J La State Med Soc 16. Aytac S, Fitoz S, Atasoy C, et al. Multimodality
1993;145:48. demonstration of primary splenic angiosarcoma. J
11. Ohtomo K, Fukuda H, Mori K, et al. CT and MR Clin Ultrasound 1999;27:92.