Background

Testicular MS is one of the rare types of MS, and our literature search shows that there is a paucity of data on TMS [1]. TMS with concomitant jejunal and retroperitoneal deposit as in our case has not been reported so far. Overall, MS has been classified into four types: (i) primary MS, (ii) MS as an extramedullary manifestation of AML, (iii) MS as isolated recurrence of AML and (iv) MS with coexisting bone marrow relapse of AML [2]. Histopathological examination with immunohistochemical testing remains the gold standard for diagnosis [3].

Case presentation

A 28-year-old gentleman presented with complaints of abdominal pain and constipation since 1 month with dull dragging type of scrotal pain. Ultrasound scrotum showed left extratesticular hyperechoic mass extending intraabdominally along the spermatic cord with bilateral chronic hydrocele (Fig. 1). Initial CT abdomen revealed left testicular vein thrombosis and retroperitoneal lymphadenopathy causing obstructive grade 2 left hydroureteronephrosis (Fig. 2a–c) with transient jejunojejunal intussusception (Fig. 3a, b). Blood workup showed elevated LDH (356). Patient was then subjected to high-resolution MRI scrotum and abdomen in 3 Tesla scanner (Skyra, Siemens, Healthineers, Erlangen, Germany) which showed enlarged left testis with altered signal intensity, diffusion restriction and a left extratesticular mass (Fig. 4a, b). Left spermatic cord was thickened (Fig. 4c), with large retroperitoneal nodal mass abutting the gonadal vessels and compressing the ureter (Fig. 5a, b). A diagnosis of testicular lymphoma with retroperitoneal and small bowel deposit was made, and left high inguinal orchidectomy was done with left ureteric DJ stenting (Fig. 6a). IHC was positive for CD99, CD34, CD45, MPO, Ki 67–90%. Pathological diagnosis of granulocytic sarcoma was made (Fig. 6b).

Fig. 1
figure 1

High frequency ultrasound scrotum showing ill-defined extra testicular mass (arrow) with chronic hydrocele

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Fig. 2
figure 2

a–c Intravenous contrast CT pelvis axial and coronal sections of abdomen and pelvis showing heterogeneously enhancing left testis (green arrow) with retroperitoneal nodal deposit abutting the gonadal vessel and compressing the ureter (yellow arrow) with delayed nephrogram (white arrow)

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Fig. 3
figure 3

a, b CT abdomen with oral contrast showing circumferential wall thickening in jejunum causing luminal obstruction (yellow arrow) was initially presented as jejunojejunal intussusception (white arrow) with circumferential mass as a lead point

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Fig. 4
figure 4

a–c High-resolution MRI scrotum (T1, T2 sagittal and STIR coronal) showing T2 hyperintense bilateral hydrocele with T1 hypo- and T2 hyperintense extratesticular mass with thickened spermatic cord extending intraperitoneally

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Fig. 5
figure 5

a, b TRUFI, HASTE abdomen coronal showing multiple enlarged para-aortic lymph nodes abutting left gonadal vessels

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Fig. 6
figure 6

a–c Intraoperative and histopathological image of left testis and small bowel deposit showing neoplastic cells which are positive for CD99, CD34, CD45, MPO, Ki 67–90%

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1 month later during postoperative follow-up, patient presented with acute abdomen pain. CT abdomen done with oral contrast revealed circumferential wall thickening in jejunum causing complete small bowel obstruction. Conservative jejunojejunostomy was done (Fig. 6c) with retroperitoneal nodal mass biopsy which showed myeloid sarcoma deposits (MPO positive). Though blood counts were normal initially, a hematological workup was made to rule out AML which commonly precedes GS. Peripheral smear showed 9% blast cells and 12% atypical cells and thrombocytopenia. Bone marrow IHC markers came positive for CD34, 45, 13, 33, 117 and MPO strongly positive, and hence, the diagnosis of AML was made.

Follow-up: Patient started on chemotherapy as a palliative treatment.

Discussion

Granulocytic sarcoma is a rare extramedullary tumor composed of immature granulocytic precursors commonly associated with AML, CML, polycythemia vera, myelofibrosis. Rarely, it may manifest as a primary presentation before the onset of systemic disease in acute myeloid leukemia [4, 5]. We should offer them as a differential for timely workup and early diagnosis.

Granulocytic sarcoma lesions will be multiple and solid, recurring at different sites. The central nervous system, subcutaneous tissues and genitourinary system are the most common sites of disease.

At immunohistochemical staining of MS, CD68, lysozyme and CD43 are the most widely expressed markers with variable expression of a wide range of other antigens, including myeloperoxidase, CD33, CD34, CD117 (c-Kit), etc. MRI imaging features of soft-tissue granulocytic sarcoma masses are largely isointense and mildly hyperintense appearing on T1- and T2-weighted MR imaging, respectively, with variable degrees of enhancement which is difficult to differentiate from carcinoma and lymphoma. Another differential will be abscess in which the mass will be peripherally enhancing with central T1 hypo- and T2 hyperintensity with diffusion restriction. Signs strongly suggestive of granulocytic sarcoma are multiple, enhancing, solid masses occurring at different sites and time points during the course of disease in a patient with either acute myeloid leukemia or myeloproliferative or myelodysplastic disorders. Median survival period after the diagnosis of MS is 7.5 months (range 1–41 months) [6].

Conclusions

Myeloid sarcoma of testis can mimic other testicular tumors like lymphoma and metastasis. A high index of suspicion may be warranted in instances where multifocal lesions are observed in various sites as in our case to suggest this rare diagnosis and may be offered as a differential diagnosis to facilitate further workup.