|
 
 |
| LETTER TO EDITOR |
|
| Year : 2020 | Volume
: 40
| Issue : 3 | Page : 147-148 |
|
Intramuscular metastasis of renal cell carcinoma: A rare occurrence, diagnosed on fine-needle aspiration cytology
Mona A Agnihotri, Kanchan S Kothari, Leena P Naik
Department of Pathology, Seth G.S. Medical College and KEM Hospital, Mumbai, Maharashtra, India
| Date of Submission | 21-Sep-2019 |
| Date of Decision | 28-Nov-2019 |
| Date of Acceptance | 31-Jan-2020 |
| Date of Web Publication | 04-Mar-2020 |
Correspondence Address:
Dr. Mona A Agnihotri
Department of Pathology, Seth G.S. Medical College and KEM Hospital, Parel, Mumbai - 400 012, Maharashtra
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/jmedsci.jmedsci_161_19
How to cite this article:
Agnihotri MA, Kothari KS, Naik LP. Intramuscular metastasis of renal cell carcinoma: A rare occurrence, diagnosed on fine-needle aspiration cytology. J Med Sci 2020;40:147-8 |
How to cite this URL:
Agnihotri MA, Kothari KS, Naik LP. Intramuscular metastasis of renal cell carcinoma: A rare occurrence, diagnosed on fine-needle aspiration cytology. J Med Sci [serial online] 2020 [cited 2022 Aug 19];40:147-8. Available from: https://www.jmedscindmc.com/text.asp?2020/40/3/147/280014 |
Dear Sir,
Renal cell carcinoma (RCC) is associated with aggressive behavior and a strong tendency for metastatic spread.[1] The common metastatic sites are lungs, liver, bone, and brain, while the rare sites are head and neck, heart, skin, ovaries, uterus, testis, and joints.[1] Skeletal muscle metastasis is an unusual occurrence and its prevalence is just 1.6%.[2],[3]
A 41-year-old male presented with a rapidly growing swelling located in the posterior compartment of the left arm, for 2 months. It measured 4 cm × 2 cm in size and was firm, slightly tender, and free from the overlying skin. On ultrasonography (USG), a hypoechoic highly vascular lesion was seen within the head of triceps, and a diagnosis of neural tumor, possibly malignant, was suggested. Aspiration under USG guidance was done, following the standard procedure using a 24-G needle and a 10 cc syringe. Hemorrhagic material was obtained. Both air-dried and alcohol-fixed smears were made and stained with Giemsa and Papanicolaou stains, respectively. The smears were moderately cellular with a hemorrhagic background and comprised loosely cohesive clusters of cells adhering to thin strands of myxoid stroma [Figure 1]a. The myxoid stroma was easily identified as magenta-colored wispy strands on Giemsa smears. The cells were large and had abundant pale cytoplasm with fine vacuolations while occasional showed granular cytoplasm [Figure 1]a and [Figure 1]b. The nuclear-cytoplasmic ratio was low, the nuclei were moderately pleomorphic, and few showed prominent nucleoli [Figure 1]b. Occasional intranuclear cytoplasmic inclusions were also seen. The cytomorphologic appearance was very typical of RCC, and on questioning, the patient gave a history of a nephrectomy done 6 years back. The old report was retrieved by the patient, and it showed grade 1 clear cell RCC. Subsequently, the patient underwent a positron emission tomographic scan that showed metastasis in the ribs and lungs as well. He was put on sunitinib, and 8 months later, the arm swelling had disappeared while those in ribs and lungs had decreased in size. | Figure 1: (a) Cells displaying abundant cytoplasm with fine vacuolations and adherent to fine strand of stromal material (Giemsa, ×400). (b) Cell showing intranuclear inclusion (Giemsa stain, ×400)
Click here to view |
Majority of RCC are histologically of the classic clear cell type.[4] The diagnostic cytomorphological feature is the loosely cohesive clusters of pale vacuolated cells with low nuclear-cytoplasmic ratio adhering to the fine strands of myxoid stromal material. The fibrillary stroma probably represents the delicate vasculature within the tumor and appears magenta in colour with May Grunwald Giemsa (MGG) stain.[4],[5] These findings are better appreciated in low and intermediate grade as compared to poorly differentiated end of the spectrum. The background is typically hemorrhagic. 4 It is the occurrence at unusual sites that often becomes a diagnostic challenge for a cytologist, especially in the absence of history, and needs to be differentiated from other primary and metastatic clear cell tumors common at that site.[5] Likewise, in the current case of intramuscular lesion located at arm, it should be differentiated from clear cell sarcoma (CSS), adnexal tumors with clear cell morphology, and metastasis of other clear cell carcinomas.[5] CSS is usually located around the knee, commonly occurs in young adults, shows dispersed oval cells with large prominent nucleoli on cytology, and is positive for melanocytic lineage markers, such as S-100 and HMB-45.[5] Most adnexal tumors are superficial and skin is not pinchable. Sebaceous carcinoma additionally shows abundant, variable-sized intracellular and extracellular lipid vacuoles.[5] Metastasis from other sites of primary malignancy such as lung and colon can be differentiated on the basis of the characteristic cytomorphology of RCC, and immunocytochemistry would be of help in cases of difficulty. A simultaneous expression of keratin and vimentin is diagnostic for the renal origin of tumor. Care must also be taken not to mistake the cells of a low-grade tumor for histiocytes, and careful attention to the nuclear morphology is important.
The present case thus highlights the classical morphology of RCC and also its propensity for metastasis to unusual sites.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient has given his consent for his images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
| References | |  |
| 1. | Sountoulides P, Metaxa L, Cindolo L. Atypical presentations and rare metastatic sites of renal cell carcinoma: A review of case reports. J Med Case Rep 2011;5:429.  |
| 2. | Sakamoto A, Yoshida T, Matsuura S, Tanaka K, Matsuda S, Oda Y, et al. Metastasis to the gluteus maximus muscle from renal cell carcinoma with special emphasis on MRI features. World J Surg Oncol 2007;5:88. |
| 3. | D'Elia C, Cai T, Luciani L, Bonzanini M, Malossini G. Pelvic and muscular metastasis of a renal cell carcinoma: A case report. Oncol Lett 2013;5:1258-60. |
| 4. | Renshaw AA, Cibas ES. Kidney and adrenal gland. In: Cibas ES, Ducatman BS, editors. Cytology Diagnostic Principles and Clinical Correlates. Philadelphia: Elsevier Saunders; 2014. p. 423-51. |
| 5. | Dhingra V, Misra V, Singh AP, Agarwal S. Cytodiagnosis of cutaneous metastasis from renal cell carcinoma: A case report with review of literature. J Cytol 2011;28:30-2. [ PUBMED] [Full text] |
[Figure 1]
|
Search Pubmed for