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1.
São Paulo med. j ; 136(6): 586-590, Nov.-Dec. 2018. tab, graf
Article in English | LILACS | ID: biblio-991690

ABSTRACT

ABSTRACT BACKGROUND: Malignant transformation of endometriosis in the abdominal wall is a rare and still poorly understood event. Less than 30 cases have been reported in the worldwide literature. Most cases of solid tumors are report in a previous abdominal scar with malignant transformation of a focus of endometriosis. Presence of lymph node metastases in nearby chains is frequent and is associated with poor prognosis. CASE REPORT: We report a case of a 42-year-old woman with a history of abdominal surgery (Pfannenstiel) to resect abdominal wall endometriosis. Physical examination revealed a solid mass of approximately 10 cm x 6 cm in the anterior wall of the abdomen. Computed tomography (CT) of the abdomen and pelvis showed a heterogeneous, predominantly hypoattenuating expansive formation measuring 10.6 cm x 4.7 cm x 8.3 cm. The patient underwent exploratory incisional laparotomy, block resection of the abdominal mass and lymphadenectomy of the external and inguinal iliac chains. The abdominal wall was reconstructed using a semi-absorbable tissue-separating screen to reconstitute the defect caused by resection of the tumor. Histological evaluation revealed infiltration by malignant epithelioid neoplasia, thus confirming the immunohistochemical profile of adenocarcinoma with clear cell components. Lymphadenectomy showed metastatic involvement of an external iliac chain lymph node. CONCLUSION: Resection of the mass along with the abdominal wall, with wall margins, is the most effective treatment. Reconstruction is a challenge for surgeons. The patient has been followed up postoperatively for eight months, without any evidence of disease to date.


Subject(s)
Humans , Female , Adult , Cell Transformation, Neoplastic/pathology , Adenocarcinoma, Clear Cell/etiology , Endometriosis/complications , Lymphatic Metastasis/pathology , Abdominal Neoplasms/etiology , Tomography, X-Ray Computed , Adenocarcinoma, Clear Cell/surgery , Adenocarcinoma, Clear Cell/pathology , Neoadjuvant Therapy , Abdominal Wall/surgery , Lymph Node Excision , Abdominal Neoplasms/surgery , Abdominal Neoplasms/pathology
2.
J. appl. oral sci ; 26: e20160645, 2018. graf
Article in English | LILACS, BBO | ID: biblio-893726

ABSTRACT

Abstract Clear cell odontogenic carcinoma (CCOC) is a rare odontogenic tumor of the jaws, histologically characterized by the presence of agglomerates of cells with eosinophilic cytoplasm. The patient, a 62-year-old Caucasian woman, presented an intraosseous lesion in the mandibular symphysis. A clinical examination revealed a discrete volumetric increase with a hard consistency, palpable to extraoral and intraoral examinations. Imaging studies revealed an extensive radiolucent area, without defined limits, extending from the region of the right second premolar to the left canine. Incisional biopsy analysis indicated a diagnosis of CCOC. The treatment proposed was segmental resection of the mandible with a safety margin. After six months without recurrence, definitive mandibular reconstruction was performed using an iliac crest graft, followed by rehabilitation with implant-supported denture after five months. After three years of post-resection follow-up, the patient has shown no evidence of recurrence or metastasis. She continues to be under follow-up. To conclude, CCOC must be considered a malignant tumor with aggressive behavior. Previous studies have shown that resection with free margins is a treatment with a lower rate of recurrence. Nevertheless, long-term follow-up is necessary for such patients.


Subject(s)
Humans , Female , Mandibular Neoplasms/surgery , Odontogenic Tumors/surgery , Adenocarcinoma, Clear Cell/surgery , Biopsy , Radiography, Panoramic , Mandibular Neoplasms/pathology , Mandibular Neoplasms/diagnostic imaging , Odontogenic Tumors/pathology , Odontogenic Tumors/diagnostic imaging , Bone Transplantation/methods , Treatment Outcome , Adenocarcinoma, Clear Cell/pathology , Adenocarcinoma, Clear Cell/diagnostic imaging , Mandibular Osteotomy/methods , Ilium/transplantation , Middle Aged
3.
Indian J Pathol Microbiol ; 2012 Apr-Jun 55(2): 245-247
Article in English | IMSEAR | ID: sea-142234

ABSTRACT

We present a rare case of clear cell adenocarcinoma of the male bulbomembranous urethra. Mostly these tumors have been described in the female urethral tract with its possible origin from mullerian remnants, wolffian remnants or paraurethral glands. Histologically, these tumors have typically tubulocystic pattern comprising of hobnailed cells with clear glycogenated cytoplasm along with well-defined cytoplasmic membranes. This case is being presented due to its rarity, aggressive behavior and to discuss, trauma as its possible etiological factor


Subject(s)
Adenocarcinoma, Clear Cell/diagnosis , Adenocarcinoma, Clear Cell/pathology , Adenocarcinoma, Clear Cell/surgery , Histocytochemistry , Humans , Magnetic Resonance Imaging , Male , Microscopy , Middle Aged , Penis/pathology , Penis/diagnostic imaging , Urethral Neoplasms/diagnosis , Urethral Neoplasms/pathology , Urethral Neoplasms/surgery
4.
Indian J Pathol Microbiol ; 2011 Jan-Mar 54(1): 167-169
Article in English | IMSEAR | ID: sea-141946

ABSTRACT

Hyalinizing clear cell carcinoma (HCCC) of tongue is a rare neoplasm originating from minor salivary glands. We present a case of HCCC involving the base of tongue, in a 73-year-old male, clinically diagnosed as fibroma. Laser excison of the mass was done. Histopathological examination showed an infiltrating lesion composed predominantly of clear clear. The differential diagnosis included other salivary gland lesions having a clear cell component and metastatic clear cell renal carcinoma. lmmunohistochemistry was useful in ruling out these lesions exhibiting clear cell component from clear cell carcinoma. imaging studies revealed no lesion in either kidney. Since, HCCC has a better prognosis and the adequate treatment is wide excision, it needs to be differentiated from other carcinomas with clear cells. No further therapy was given to the patient. One year after the surgery, the patient is symptom free without local recurrence and on regular follow up.


Subject(s)
Adenocarcinoma, Clear Cell/diagnosis , Adenocarcinoma, Clear Cell/pathology , Adenocarcinoma, Clear Cell/surgery , Aged , Endoscopy , Histocytochemistry , Humans , Hyalin/metabolism , Immunochemistry , Laser Therapy , Male , Microscopy , Tongue/pathology , Tongue/surgery , Tongue Neoplasms/diagnosis , Tongue Neoplasms/pathology , Tongue Neoplasms/surgery
5.
Cir. & cir ; 76(4): 339-342, jul.-ago. 2008. ilus
Article in Spanish | LILACS | ID: lil-568076

ABSTRACT

BACKGROUND: Renal cell carcinoma (RCC) represents approximately 3% of malignant tumors in adults and occurs in a M:F ratio of 1.5:1.0. Although in most cases it occurs in persons 50 to 70 years of age, there are also reports in children. Clear cell carcinoma is the most frequent histological type, and 30% of renal carcinomas have metastasized at the time of diagnosis. The objective of the present study is to report colon metastasis of clear cell carcinoma that required surgery and chemotherapy. CLINICAL CASE: We report the case of a 60-year-old male with a history of metastatic RCC. His treatment consisted of cytoreductive radical nephrectomy and interferon because of pulmonary disease. He was followed-up for 8 years. Nevertheless, he presented with hematochezia and underwent colonoscopy where a splenic flexure tumor was demonstrated. Biopsy reported a clear cell tumor. We performed a left hemicolectomy. Pathology report was clear cell carcinoma with involvement of the colon from the mucosa to serosa. The patient again received interferon. Currently, there is no evidence of tumor activity and the patient is being followed-up. CONCLUSIONS: RCC metastases are most frequent in lung, liver, and bone and less frequent in brain, skin, and soft tissue. Metachromic metastases are identified in the first to second year after nephrectomy in most cases. Survival of patients who present metastasis <1 year after nephrectomy is 33 months vs. patients who present metastasis after 1 year from nephrectomy (55 months). Metastatic clear cell carcinoma requires surgery and immunotherapy. Surgery is the first step for disease control and metastatecomies are indicated in localized disease or when one organ is affected and surgically accessible.


Subject(s)
Humans , Male , Middle Aged , Adenocarcinoma, Clear Cell/secondary , Carcinoma, Renal Cell/secondary , Kidney Neoplasms/pathology , Colonic Neoplasms/secondary , Adenocarcinoma, Clear Cell/drug therapy , Adenocarcinoma, Clear Cell/surgery , Antineoplastic Agents/therapeutic use , Combined Modality Therapy , Carcinoma, Renal Cell/complications , Carcinoma, Renal Cell/drug therapy , Carcinoma, Renal Cell/surgery , Colectomy/methods , Follow-Up Studies , Gastrointestinal Hemorrhage/etiology , Immunotherapy , Interferon-alpha/therapeutic use , Nephrectomy/methods , Lung Neoplasms/secondary , Kidney Neoplasms/drug therapy , Kidney Neoplasms/surgery , Colonic Neoplasms/complications , Colonic Neoplasms/drug therapy , Colonic Neoplasms/surgery , Remission Induction
6.
Journal of Korean Medical Science ; : 217-219, 1999.
Article in English | WPRIM | ID: wpr-149185

ABSTRACT

Endometriosis of a surgical scar is rare and occurs mainly when a hysterectomy or Cesarean section was performed. We describe a 54-year-old woman with a large suprapubic mass as a definite case of a endomerioid carcinoma developing within the scar endometriosis following Cesarean section. Scar endometriosis, as well as endometriosis at other sites, can turn malignant. Endometrioid carcinoma is the most common histological pattern of malignant tumor arising in endometriosis. But clear cell carcinoma is very unusual. A case of primary clear cell carcinoma in endometriosis of a Cesarean section scar is described. To the best of our knowledge, this is the first documented case of endomerioid carcinoma developing within the scar endometriosis in Korea.


Subject(s)
Female , Humans , Adenocarcinoma, Clear Cell/surgery , Adenocarcinoma, Clear Cell/pathology , Adenocarcinoma, Clear Cell/etiology , Carcinoma, Endometrioid/surgery , Carcinoma, Endometrioid/pathology , Carcinoma, Endometrioid/etiology , Cesarean Section/adverse effects , Cicatrix , Endometriosis/physiopathology , Middle Aged , Tomography, X-Ray Computed/methods
7.
J. bras. patol ; 34(4): 304-6, out.-dez. 1998. ilus
Article in English | LILACS | ID: lil-229587

ABSTRACT

Os autores relatam um caso de carcinoma basocelular de células claras, que acreditam ser o primeiro caso brasileiro. A importância desta rara variante e seu diagnóstico diferencial histopatológico säo resaltados, após breve discussäo da literatura


Subject(s)
Humans , Female , Middle Aged , Adenocarcinoma, Clear Cell/surgery , Adenocarcinoma, Clear Cell/diagnosis , Carcinoma, Basal Cell/diagnosis , Carcinoma, Basal Cell/surgery , Diagnosis, Differential
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