scholarly journals Immunohistochemical characteristics of renomedullary interstitial cell tumor: a study of 41 tumors with emphasis on differential diagnosis of mesenchymal neoplasms

2018 ◽  
Vol 82 ◽  
pp. 46-50
Author(s):  
Zhichun Lu ◽  
Khaleel Al-Obaidy ◽  
Liang Cheng ◽  
Kyle D. Perry ◽  
David J. Grignon ◽  
...  
2004 ◽  
Vol 128 (12) ◽  
pp. 1442-1444 ◽  
Author(s):  
Katherine M. Ceballos ◽  
Julie-Ann Francis ◽  
John L. Mazurka

Abstract Gastrointestinal stromal tumors are CD117 (c-Kit)–positive mesenchymal neoplasms with histologic and ultrastructural features of the interstitial cell of Cajal. While tumors outside of the gastrointestinal tract have been described, to our knowledge the case we present is the first such case in the vagina. We describe a 75-year-old woman with a recurrent vaginal gastrointestinal stromal tumor without apparent rectal involvement. This tumor was characterized by short intersecting fascicles of spindled cells, focal necrosis, and 12 to 15 mitoses per 50 high-power fields. Immunohistochemistry revealed diffuse cytoplasmic positivity for CD117 (c-Kit), CD34, vimentin, and h-caldesmon. Tumor cells were negative for S100, desmin, actin, and CAM 5.2. The differential diagnosis in this case included a vaginal smooth muscle tumor. While histologically similar to a smooth muscle neoplasm, the immunohistochemical profile ruled out smooth muscle differentiation. Gastrointestinal stromal tumor should be considered in the differential diagnosis of vaginal mesenchymal neoplasms.


2019 ◽  
Vol 47 ◽  
Author(s):  
Halan Hallamys De Lima Nascimento ◽  
Camila Tochetto ◽  
Ricardo Barbosa Lucena ◽  
Glaucia Denise Kommers

Background: Although testicular tumors commonly develop in the genital tract of dogs, only few studies have reported about metastatic testicular tumors in dogs to date. Therefore, the present study aimed to describe the gross, histopathological, and immunohistochemical findings in a dog with metastatic interstitial cell tumor.Case: A 6-year-old male Beagle underwent clinical examination due to enlargement of the left testicle and nodules in the skin of the left inguinal region and of the scrotum. The left testicle was cryptorchid (inguinal), and the right testicle was intrascrotal. Both testicles and affected skin fragments were surgically removed. The right testicle was normal in size and did not exhibit gross changes. However, the left testicular parenchyma had been completely replaced by a firm, grayish-to-white neoplastic mass with an irregular surface. The inguinal and scrotal skin fragments were thickened by the neoplastic masses. Histologically, the left testicular parenchyma was completely obliterated by a neoplastic mass consisting of round-to-oval and polygonal cells. The neoplastic cells generally had abundant eosinophilic cytoplasm with indistinct cell limits. The nuclei were round and small, with aggregated chromatin. However, some cells exhibited high degrees of atypia and pleomorphism and large nuclei with granular chromatin. Mitotic figures were observed at high frequencies of up to 11 per high-power field (400×). The mass in the left testicle was diagnosed as malignant interstitial cell tumor. The sections of the inguinal skin and scrotum presented with neoplastic cells similar to those observed in the left testicle, which is consistent with the metastasis of the malignant testicular interstitial cell tumor. On the basis of necropsy, multiple cutaneous and subcutaneous nodules were randomly distributed throughout the body, primarily in the prepuce, head, and limbs. Histological evaluations of the skin nodules, internal iliac lymph nodes, and abdominal skeletal muscles also revealed metastases of the testicular interstitial cell tumor.Discussion: The histopathological findings associated with the immunohistochemical results observed in the present case helped in establishing the diagnosis of malignant interstitial cell tumor. Regarding the histological evaluations, although most neoplastic cells exhibited appearances that are characteristic of Leydig cells, several features indicative of malignancy were also observed. In dogs, malignant interstitial cell tumors are rare, and multiple organ metastases have been described. Among the immunohistochemical markers that were examined (calretinin, vimentin, cytokeratin, placental alkaline phosphatase, and octamer-binding transcription factor 3/4), only vimentin staining produced a positive result. In one study, the antibody against vimentin stained both normal Sertoli and Leydig cells and tumors arising from these cells, but not seminomas, which is an important differential diagnosis in the case described in this study. The negativity for placental alkaline phosphatase also allowed to rule out seminoma in the differential diagnosis of the primary tumor. The skin sections (distant metastases) were negative for T and B lymphocytes and macrophages, thereby ruling out possible differential diagnoses, such as lymphomas or histiocytic tumors, among the cutaneous neoplasms. Therefore, this case report described a malignant testicular interstitial cell tumor with an uncommon disseminated pattern of metastases to the skin in a dog.


2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Sawsan Ismail ◽  
Munawar Hraib ◽  
Rana Issa ◽  
Thanaa Alassi ◽  
Zuheir Alshehabi

Abstract Background Ovarian steroid cell tumors represent a rare category of sex cord-stromal tumors that constitute less than 0.1% of all ovarian tumors. These neoplasms are classified into three main subtypes according to the cell of origin: Leidyg cell tumors, stromal luteomas, and steroid cell tumors not otherwise specified (SCTs-NOS). The latter subtype is defined as a neoplasm of an uncertain lineage that mostly affects middle-aged women, whereas it’s rare in younger ages. Case presentation We report a case of a 21-year-old virgin female who presented to our hospital with complaints of mild abdominal pain, hirsutism, and oligomenorrhea for more than a year. Before her current admission, the patient had attended an external gynecologic clinic where she had been prescribed oral contraceptives to regulate her periods. Nevertheless, on presentation to our institution, physical examination revealed abdominal tenderness with a palpable pelvic mass and mild hirsutism in the thigh. Ultrasonography demonstrated a large left ovarian mass measuring 154 × 104 mm, and compressing the uterus. Therefore, a unilateral salpingo-oophorectomy was performed, and interestingly, pathologic examination of the large aforementioned mass alongside with immunohistochemical correlation revealed the diagnosis of a large ovarian steroid cell tumor-not otherwise specified with a unique combination of benign and malignant features. Conclusions Although ovarian steroid cell tumors represent a rare category, they must be considered in the differential diagnosis for mild virilization symptoms in young females due to the importance of early diagnosis and management. In this manuscript, we aimed to present the first case report from Syria that highlights the crucial role of detailed morphological examination for challenging cases despite the difficulties in differential diagnosis, and the absence of ancillary techniques. Furthermore, we managed to discuss a brief review of diagnostic methods, histological characteristics, and treatment recommendations.


2015 ◽  
Vol 10 (5) ◽  
pp. 2991-2995 ◽  
Author(s):  
YUAN CAO ◽  
YING CHEN ◽  
LI YANG ◽  
ZI-HUA QIAN ◽  
SHU-GAO HAN ◽  
...  

2008 ◽  
Vol 32 (2) ◽  
pp. 161
Author(s):  
W Yang ◽  
M.-H Chen ◽  
K Yan ◽  
W Wu ◽  
Y Dai ◽  
...  

1953 ◽  
Vol 69 (4) ◽  
pp. 562-570 ◽  
Author(s):  
William J. Staubitz ◽  
Oscar J. Oberkircher ◽  
Michael S. Blick

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