Professional Documents
Culture Documents
Abdom CT in AIDS AJR 1986
Abdom CT in AIDS AJR 1986
R. Brooke Jeffrey, Jr.1 Acquired immunodeficiency syndrome (AIDS) is a lethal infectious disease that has
David A. Nyberg1’2 reached epidemic proportions in urban centers of the United States. lntraabdominal
Kent Bottles3 opportunistic infections and malignancies are common features of this syndrome. A
Donald I. Abrarns4 prodromal phase or possibly milder form of infection is known as the AIDS-related
complex. Abdominal computed tomography (CT) in patients with AIDS-related complex
Michael P. Federl&
often demonstrates a triad of mild retroperitoneal and mesentenc adenopathy, spleno-
Susan D. Wall1 megaly, and perirectal inflammation. Lymph node enlargement greater than 1.5 cm is
Vivian W. Wing1 unusual in the AIDS-related complex and should prompt CT-guided biopsy. Abdominal
Faye C. Laing1 adenopathy (>1.5 cm) in AIDS, in our experience, is most commonly related to non-
Hodgkin lymphoma, Kaposi sarcoma, or infection with Mycobacterlum avlum-Intracellu-
lare. In most instances, CT-guided biopsy with appropriate staining technique can readily
distinguish these entities. However, the subtyping of non-Hodgkin lymphoma by fine-
needle aspiration biopsy alone remains controversial. Unusual features of abdominal
malignancies are common in AIDS. These include a purely lymphadenopathic form of
AIDS-related Kaposi sarcoma and a predilection for extranodal sites
in of lymphoma
AIDS. In general, patients with AIDS-related lymphoma present with advanced stages of
disease with highly malignant histologic subtypes. Abdominal CT may be useful clinically
for diagnosing intraabdominal complications of AIDS.
enlargement may be the only CT evidence of abdominal rarely seen on CT, larger focal masses may be identified by
Kaposi sarcoma. Indeed a purely lymphadenopathic form of mural thickening (fig. 4). The CT demonstration of focal he-
AIDS-related Kaposi sarcoma is being recognized with in- patic or splenic lesions of Kaposi sarcoma in AIDS is uncom-
creasing frequency [21, 22] (fig. 3). This is an interesting mon. As with retroperitoneal adenopathy, this sarcoma has a
clinical correlate to the growing histochemical evidence of the nonspecific CT appearance and cannot be distinguished from
origin of Kaposi sarcoma from lymphatic endothelial cells other neoplastic or infectious causes without FNAB. In our
[23]. Without FNAB, it is not possible to distinguish bulky experience, FNAB has proven quite reliable in diagnosing
adenopathy in AIDS-related Kaposi sarcoma from lymphoma AIDS-related Kaposi sarcoma [24]. Cohesive clusters of bland
or infections such as Mycobacterium avium-intracellulare. spindle cells are arranged in characteristic slitlike spaces
Although the characteristic “target” Kaposi sarcoma lesions [24]. Because Kaposi sarcoma can involve virtually any organ
seen on air-contrast studies of the gastrointestinal tract are in the body, it may produce unusual intraabdominal lesions
10 JEFFREY ET AL. AJR:146, January 1986
Fig. 7.-Small hepatic lesions in non-Hodgkin lymphoma. A, Marked hepa- B, Hepatic sonogram. Diffuse distortion of echogenicity and numerous focal
tomegaly but only two focal abnormalities on contrast-enhanced CT (arrows). lesions (arrows).
8.-Cytomegalovirus enteritis and colitis. A, L..fuse small-bowel (B) wall thickening and mucosal irregularity. B, Mesenteric adenopathy (n) and pancolitis
with focal narrowing of lumen and mural thickening of the colon (C).
inal CT, M. avium-intracellulare has a high predilection for biopsy to exclude M. avium-intracellulare, despite an unre-
retroperitoneal and mesenteric nodal involvement, producing markable CT scan.
bulky nodal masses that are often indistinguishable from On CT, low-density areas of necrosis may occasionally be
AIDS-related Kaposi sarcoma or lymphoma (fig. 10). In our identified within abdominal lymph nodes involved with M.
series of 17 patients with proven abdominal M. avium-intra- avium-intrace!lulare (fig. 12). FNAB in M. avium-intracellulare
cellulare, 14 (82%) had mesenteric or retroperitoneal ada- can readily detect macrophages laden with acid-fast bacilli,
nopathy greater than 1.0-1.5 cm on CT [36]. Focal hepatic and thus acid-fast stains should be routinely performed in all
and splenic lesions were identified by CT or sonography in FNAB specimens in AIDS. Unfortunately, at present there is
two patients (fig. 11). We recently encountered a patient with no effective medical therapy for M. avium-intracellulare.
diffuse hepatic M. avium-intracellulare on liver biopsy without Rectal and perirectal inflammatory disease are common
focal defects on CT. Therefore, AIDS patients with persistent both in patients with the AIDS-related complex and in those
abnormal liver functions and fever may require core liver with AIDS. Proctitis is often secondary to venereal infections
12 JEFFREY ET AL. AJR:146, January 1986
from gcnococci, syphilis, cytomegalovirus, herpes simplex, or lu/are, abdominal or pelvic abscesses, and diagnosis and
lymphogranuloma venereum. In some instances it may be staging of abdominal neoplasms such as Kaposi sarcoma and
difficult to distinguish rectal Kaposi sarcoma or lymphoma lymphoma. In patients with localized symptoms such as right-
from severe proctitis. CT seems to be of considerable value upper-quadrant pain, sonography is often a useful initial
in distinguishing perirectal cellulitis from abscesses and local- screening method. On occasion, sonography may reveal sub-
izing complex abscesses before surgical drainage (Guillaumin tle hepatic lesions difficult to image by CT. Because of the
E, unpublished data). frequency of mesenteric retroperitoneal nodal disease in
AIDS, CT remains the primary method for evaluation in most
patients. Although chemotherapy for AIDS-related neoplasms
Indications for Abdominal CT in AIDS
is often limited in its effectiveness, repeat abdominal CT is
Indications for abdominal CT in AIDS include evaluation for often useful to assess the course of therapy.
suspected visceral or nodal infection with M. avium-intracel-
REFERENCES
1 . Gottlieb MS, Schroff R, Schanker H, et al. Pneumocystitis carinll
pneumonia and mucosal candidiasis in previously healthy ho-
mosexual men: evidence of a new acquired cellular immunode-
ficiency. N EnglJ Med 1981;305:1425-1431
2. Centers for Disease Control. Kaposi’s sarcoma and pneumocys-
tis pneumonia among homosexual men-New York City and
California. MMWR 1981;30:305-308
3. Masur H, Michelis MA, Greene JB, et al. An outbreak of corn-
rnunity-acquired Pneumocystis carinii pneumonia: initial rnanifes-
tation of cellular immune dysfunction. N EngI J Med
1981;305:1431-1438
4. Jaffe HW, Bregrnan DJ, Selik RM. Acquired immune deficiency
syndrome in the United States: the first 1 000 cases. J Infect Dis
1982;1 48:339-345
5. Landesman SH, Ginzburg HM, Weiss SH. Special report: the
AIDS epidemic. N EngI J Med 1985;31 2:521-524
6. Barre-Sinoussi F, Chermann JC, Rey F, et al. Isolation of a T
lymphotropic retrovirus from a patient at risk for acquired immune
deficiency syndrome (AIDS). Science 1983;220:868-871
7. Gallo RC, Salahuddin SZ, Popovic M, et al. Frequent detection
and isolation of cytopathic retroviruses (HTLV-llI) from patients
AIDS and pre-AIDS.
with Science 1984;224:500-503
Fig. 9.-Cytomegalovirus peritonitis with marked ascites. Inflammatory infil-
tration of omentum (arrow). 8. Laurence J, Brun-Vezinet F, Schutzer 5, et al. Lymphadenopa-
Fig. 1 0.-Mycobacterium avium-intracellulare infection producing bulky ret- Fig. 12.-Necrotic lymph node from Mycobacterium avium-intracellulare
roperitoneal adenopathy (N). Large wedgeshaped splenic infarct (arrow). along gastrohepatic ligament (arrow).
Fig. 11.-Focal splenic lesion (arrow) in Mycobacterium avium-intracellulare.
AJR:146, January 1986 ABDOMINAL CT IN AIDS 13
thy-associated viral antibody in AIDS. N EngI J Med 23. Beckstead JH, Wood GS, Fletcher V. Evidence for the origin of
1984;31 1 :1269-1 273 Kaposi’s sarcoma from lymphatic endothelium. Am J Pathol (in
9. Centers for Disease Control. Update: acquired immunodeficiency press)
syndrome-United States. MMWR 1985;34:245-248 24. Bottles K, Cohen MB, Brodie H, Jeffrey RB, Nyberg DA, Abrams
1 0. Seligmann M, Chess L, Fahey JL, et al. AIDS-an immunologic Dl. Fine needle aspiration cytology and the differential diagnosis
evaluation. N EngI J Med 1984;1286-1292 of lymphadenopathy in homosexual males. Diagn Cytopathol (in
1 1 . Landesman SH, Ginzburg HM, Weiss SH. Special report: the press)
AIDS epidemic. N EngI J Med 1985;312:521-524 25. Centers for Disease Control. Diffuse, undifferentiated non-Hodg-
1 2. Abrams DI, Lewis BJ, Beckstead JH, Casavant CA, Drew WL. kin’s lymphoma among homosexual males-United States.
Persistent diffuse Iymphadenopathy in homosexual men: end- MMWR 1982;31 :277-279
point or prodrome? Ann Intern Med 1984;100:801-808 26. Ziegler JL, Drew WL, Miner RC, et al. Outbreak of Burkitt’s-like
13. Centers for Disease Control. Update: acquired immunodeficiency lymphoma in homosexual men. Lancet 1982;2:631-633
syndrome (AIDS)-United States. MMWR 1984;32:688-691 27. Ziegler JL, Beckstead JA, Volberding PA, et al. Non-Hodgkin’s
1 4. Selik RM, Haverkos HW, Curran JW. Acquired immune deficiency lymphoma in 90 homosexual men: relation to generalized lymph-
syndrome (AIDS) trends in the United States, 1978-1982. Am J adenopathy and the acquired immunodeficiency syndrome. N
Med 1984;76:493-500 EngI J Med 1984:31 1 : 565-570
15. Abrams DI. Lymphadenopathy syndrome in male homosexuals. 28. Schoeppel SL, Hoppe RT, Dorfman RF, et al. Hodgkin’s disease
In: Gallen JI, Fauci AS, eds. Advances in host defense mecha- in homosexual men with generalized lymphadenopathy. Ann
nisms. New York: Raven, 1985:75-97 Intern Med 1985:102:68-70
1 6. Centers for Disease Control. Persistent, generalized lymphade- 29. Burgener FA, Hamlin DJ. Histiocytic lymphoma of the abdomen:
nopathy among homosexual males. MMWR 1983;31 :249-251 radiographic spectrum. AJR 1981;137:337-342
17. Moon KL, Federle MP, Abrams Dl, Volberding P, Lewis BJ. 30. Oliver 1W, Bernardino ME, Sones PJ. Monitoring the response
Kaposi sarcoma and lymphadenopathy syndrome: limitations of of lymphoma patients to therapy: correlation of abdominal CT
abdominal CT in acquired immunodeficiency syndrome. Radiol- findings with clinical course and histologic cell type. Radiology
ogy 1984;1 50:479-483 1983;1 49’21 9-224
18. Kaposi M. Idiopathisches multiples Pigmentsarkom der Haut. 31 . Zanorza J, Ginaldi S. Computed tomography in hepatic lym-
Arch Dermatol Syphilis 1872:4:265-273 phoma. Radiology 1981;138:405-410
1 9. Taylor JP, Templeton AC, Vogel CL, Ziegler JL, Kyalwazi 5K. 32. Orell SR, Skinner JM. The typing of non-Hodgkin’s lymphoma
Kaposi’s sarcoma in Uganda: a clinico-pathologic study. Int J using fine needle aspiration cytology. Pathology 1982:14:389-
Cancer 1971;8:125-135 394
20. Rose HS, Balthazar EJ, Megebow AJ. Alimentary tract involve- 33. Gottlieb MS, Groopman JE, Weinstein WM, Fahey JL, Detels R.
ment in Kaposi sarcoma: radiographic and endoscopic findings The acquired immunodeficiency syndrome. Ann Intern Med
in 25 homosexual men. AJR 1982;139:661-666 1983:99:208-220
21. Finkbeiner WE, Egbert BM, Groundwater JR, Sageobiel RW. 34. Balthazar EJ, Megebow AJ, Fazzini E, Opulencia JF, Engel I.
Kaposis sarcoma in young homosexual men. Arch Pathol Lab Cytomegalavirus colitis in AIDS: radiographic findings in 11 pa-
Med 1982;106:261-264 tients. Radiology 1985;155:585-590
22. Abrams Dl. Lymphadenopathy syndrome in male homosexuals. 35. Nyberg DA, Federle MP, Jeffrey RB, Bottles K, Wofsy CB.
In: Gallen JI, Fauci AS, eds. Advances in host defense mecha- Abdominal CT findings of disseminated Mycobacterium avium-
nisms. New York: Raven, 1985:75-97 intracellulare infection in AIDS. AJR 1985;145:297-299